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铀(VI)与一种淡水硅藻物种相互作用的多尺度研究。

A multiscale investigation of uranium(VI) interaction with a freshwater diatom species.

作者信息

He Yihua, Sushko Vladyslav, Hübner René, Foerstendorf Harald, Steudtner Robin, Raff Johannes, Mallet Clarisse, Jeune Anne-Hélène Le, Beauger Aude, Breton Vincent, Péron Olivier, Stumpf Thorsten, Sachs Susanne, Montavon Gilles

机构信息

Laboratoire de Physique Subatomique et des Technologies Associées, Nantes, France.

Helmholtz-Zentrum Dresden-Rossendorf, Dresden, Germany.

出版信息

Sci Rep. 2025 May 31;15(1):19110. doi: 10.1038/s41598-025-93350-5.

Abstract

Diatoms are essential bio-indicators for assessing the impact of heavy metals and hazardous materials on aquatic ecosystems. This study seeks to advance our understanding of the interaction between uranium (U) and the freshwater diatom species Achnanthidium saprophilum, employing macroscopic, microscopic, and spectroscopic approaches. Bio-association experiments with hexavalent U (U(VI)) were conducted during various diatom growth phases and revealed time- and concentration-dependent U retention by the diatoms. U bio-association was observed by scanning electron microscopy and energy-dispersive X-ray spectroscopy (EDX), indicating co-localization of U with phosphorus (P). Time-resolved laser-induced fluorescence spectroscopy on U(VI)-associated diatoms suggested the formation of two adsorbed U(VI) species, whose proportions depend on the diatom growth phase. Fourier-transform infrared spectroscopy confirmed the interaction of U(VI) dominated by carboxyl groups on diatoms, while the contribution of silanol groups from the diatom frustule appeared insignificant. U bio-association experiments revealed also U incorporation into diatom cells, confirmed by transmission electron microscopy coupled with EDX. Co-localization of U with P within the vacuole was evident, suggesting co-precipitation of various metals, including U, in form of phosphates. The results of this study highlight not only the adsorption but also the internalization of U by diatoms, which influences the fate of U in aquatic ecosystems and affects its mobility and bioavailability. These findings are highly relevant for the further development of radioecological models.

摘要

硅藻是评估重金属和有害物质对水生生态系统影响的重要生物指标。本研究旨在通过宏观、微观和光谱学方法,加深我们对铀(U)与淡水硅藻嗜腐针杆藻之间相互作用的理解。在硅藻的不同生长阶段进行了六价铀(U(VI))的生物结合实验,结果表明硅藻对铀的保留具有时间和浓度依赖性。通过扫描电子显微镜和能量色散X射线光谱(EDX)观察到铀的生物结合,表明铀与磷(P)共定位。对与U(VI)相关的硅藻进行时间分辨激光诱导荧光光谱分析,结果表明形成了两种吸附的U(VI)物种,其比例取决于硅藻的生长阶段。傅里叶变换红外光谱证实了硅藻上以羧基为主的U(VI)相互作用,而硅藻壳上硅醇基的贡献似乎微不足道。铀生物结合实验还揭示了铀被纳入硅藻细胞,这一点通过透射电子显微镜结合EDX得到证实。液泡内铀与磷的共定位很明显,表明包括铀在内的各种金属以磷酸盐形式共沉淀。本研究结果不仅突出了硅藻对铀的吸附,还突出了其内化作用,这影响了铀在水生生态系统中的归宿,并影响其迁移性和生物有效性。这些发现对放射性生态模型的进一步发展具有高度相关性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/730c/12126589/9cbe7f46eb31/41598_2025_93350_Fig1_HTML.jpg

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