Tracking nickel uptake pathways in hyperaccumulator plants using a 61Ni-enriched stable isotope tracer in soil.

IF 3.8 2区 化学 Q1 BIOCHEMICAL RESEARCH METHODS
Simone Trimmel, Alexander V Epov, Nadine Abu Zahra, Tobias Berger, Thomas Prohaska, Markus Puschenreiter, Antonia Siebenbrunner, Alice Tognacchini, Stefan Wagner, Johanna Irrgeher
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Abstract

Understanding the mechanisms of nickel (Ni) uptake by hyperaccumulator plants is essential for advancing sustainable phytomanagement. In this study, saponite materials containing either isotopically natural or 61Ni-enriched Ni were synthesised and applied in RHIZOtest experiments with Odontarrhena chalcidica. The amendments were mixed with two ultramafic soils differing in Ni content, alongside a serpentinite control. Ni bioavailability and uptake were evaluated via elemental and isotopic analysis of plant digests and diffusive gradients in thin films (DGT). Stable isotope spiking with 61Ni allowed tracing of amendment-derived Ni uptake into plant tissues, even though total Ni mass fractions in planted versus unplanted soils did not indicate significant mobilisation during the 14-day growth period. Isotope pattern deconvolution (IPD) revealed clear shifts in Ni isotopic composition in both plant and DGT samples. Tracer uptake was more pronounced in the low Ni soil, with amendment-derived Ni (xamendment) contributing 19.3 ± 5.0% of total Ni in shoots, compared to 7.7 ± 1.8% in the high-Ni soil. In standard solutions containing 50 ng g-1 total Ni, isotope pattern shifts were still detectable at enrichment levels as low as 0.01% xspike (≈ 5 pg g-1 61Ni). The findings demonstrate the sensitivity of stable isotope spiking combined with IPD in the detection of subtle uptake processes, even in short-term experiments. This approach enables the differentiation of various Ni sources in soil-plant systems that would not be achievable with quantification alone, and can thereby provide new insights into how soil mineralogy influences uptake dynamics in metal-hyperaccumulating species.

利用土壤中富集镍的稳定同位素示踪剂追踪超富集植物的镍吸收途径。
了解超积累植物对镍的吸收机制对于促进植物的可持续管理至关重要。本研究合成了同位素天然或富集镍的皂化土材料,并将其应用于黄芩根瘤菌试验中。这些改良剂与两种镍含量不同的超镁铁性土壤混合,并与蛇纹岩对照。通过元素和同位素分析和薄膜扩散梯度(DGT)来评估Ni的生物利用度和吸收。尽管在14天的生长期间,种植土壤和未种植土壤的总Ni质量分数并没有显示出显著的动员,但稳定同位素的61Ni峰值可以追踪植物组织对修正源Ni的吸收。同位素模式反褶积(IPD)揭示了植物和DGT样品中Ni同位素组成的明显变化。示踪剂的吸收在低镍土壤中更为明显,修正源Ni (xamendment)贡献19.3±5.0%,而在高镍土壤中为7.7±1.8%。在含50 ng g-1总Ni的标准溶液中,当富集水平低至0.01% xspike(≈5 pg g-1 61Ni)时,仍可检测到同位素模式变化。研究结果表明,即使在短期实验中,稳定同位素峰值结合IPD在检测细微摄取过程中的敏感性。这种方法可以区分土壤-植物系统中不同的镍源,这是单独量化无法实现的,因此可以为土壤矿物学如何影响金属超积累物种的吸收动力学提供新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
8.00
自引率
4.70%
发文量
638
审稿时长
2.1 months
期刊介绍: Analytical and Bioanalytical Chemistry’s mission is the rapid publication of excellent and high-impact research articles on fundamental and applied topics of analytical and bioanalytical measurement science. Its scope is broad, and ranges from novel measurement platforms and their characterization to multidisciplinary approaches that effectively address important scientific problems. The Editors encourage submissions presenting innovative analytical research in concept, instrumentation, methods, and/or applications, including: mass spectrometry, spectroscopy, and electroanalysis; advanced separations; analytical strategies in “-omics” and imaging, bioanalysis, and sampling; miniaturized devices, medical diagnostics, sensors; analytical characterization of nano- and biomaterials; chemometrics and advanced data analysis.
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