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淡水浮游生物摄取六价铀过程中的铀同位素分馏 (U/U)。

Uranium Isotope Fractionation (U/U) during U(VI) Uptake by Freshwater Plankton.

机构信息

School of Earth and Space Exploration, Arizona State University, Tempe, Arizona 85287, United States.

Department of Earth, Ocean and Atmospheric Sciences and National High Magnetic Field Laboratory, Florida State University, Tallahassee, Florida 32306, United States.

出版信息

Environ Sci Technol. 2020 Mar 3;54(5):2744-2752. doi: 10.1021/acs.est.9b06421. Epub 2020 Feb 10.

Abstract

Uranium contamination in the environment is a serious public health concern. Biotic U(VI) reduction and nonreductive U(VI) uptake by microorganisms (e.g., U(VI) biosorption by cyanobacteria) are effective U remediation techniques. Variations of U/U have been extensively explored to track biotic U(VI) reduction in laboratory experiments and field applications. However, U isotope fractionation during nonreductive U(VI) uptake by microorganisms is poorly constrained. To investigate U isotope fractionation in this process, we cultured freshwater plankton in the presence of U(VI) and measured U/U in the culture media and biomass. We found that nonreductive U(VI) uptake by freshwater plankton fractionated U isotopes in the opposite direction compared to biotic U(VI) reduction. δU values in freshwater plankton were consistently ∼0.23 ± 0.06‰ lighter than those in dissolved U in the culture medium at various fractions of U removal (12-30%), consistent with equilibrium isotope fractionation in a closed system. The equilibrium isotope fractionation observed in our experiments possibly results from changes in coordination geometry between dissolved U(VI) in the culture media and adsorbed U(VI) on cell surfaces. Our experimental results highlight the need to consider U isotope fractionation during nonredox U(VI) uptake by microorganisms and organic matter when applying variations of U/U to track biogeochemical processes and evaluate U remediation.

摘要

铀在环境中的污染是一个严重的公共卫生问题。生物 U(VI)还原和微生物的非还原 U(VI)摄取(例如,蓝藻对 U(VI)的生物吸附)是有效的铀修复技术。U/U 的变化已被广泛用于追踪实验室实验和现场应用中的生物 U(VI)还原。然而,微生物非还原 U(VI)摄取过程中的 U 同位素分馏受到很大限制。为了研究这一过程中的 U 同位素分馏,我们在存在 U(VI)的情况下培养淡水浮游生物,并测量培养基和生物量中的 U/U。我们发现,与生物 U(VI)还原相比,淡水浮游生物的非还原 U(VI)摄取使 U 同位素分馏方向相反。在各种 U 去除分数(12-30%)下,浮游生物中的 δU 值始终比培养基中溶解 U 的 δU 值轻约 0.23 ± 0.06‰,与封闭系统中的平衡同位素分馏一致。我们实验中观察到的平衡同位素分馏可能是由于培养基中溶解 U(VI)和细胞表面吸附 U(VI)之间的配位几何形状发生变化所致。我们的实验结果强调了在应用 U/U 的变化来追踪生物地球化学过程和评估铀修复时,需要考虑微生物和有机质对非氧化还原 U(VI)摄取过程中的 U 同位素分馏。

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