Nitrate stimulated microbial and viral activity and the subsequent influence on uranium mobility in sedimentary systems

Karrie Weber, Jeffrey Westrop, Pooja Yadav, Taylor Rosso, Vincent Noel, Arjen Van Veelen, Kristen Boye, John Bargar, Xiaoqin Wu, Romy Chakraborty
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Abstract

Mobilization of naturally-occurring uranium(U) has been recognized to give rise to geogenic U groundwater contamination in aquifers. In addition to carbonate ligand complexation, nitrate has been demonstrated to play a role in controlling U mobility by altering uranium solubility through redox reactions. Nitrate is a common anthropogenic contaminant often prevalent at high concentrations in alluvial aquifers overlaying managed land. Alluvial deposition processes that form these aquifers create a lithologically heterogeneous subsurface with defined contacts between sands, silts, and clays. This leads to deposition of organic carbon and accumulation of reduced metals/radionuclides, including U(IV), in the finer grained silts and clays. The addition of high nitrate porewater into uranium-bearing alluvial aquifer silt sediments stimulated a nitrate reducing microbial community capable of catalyzing U(IV) oxidation and mobilization of U into porewaters. However, metadata from an aquifer wide study and a subsequent experiment revealed that this result is concentration dependent. Low concentrations of nitrate bearing pore-water added into organic-rich, uranium bearing sediments and resulted in a decrease in dissolved U(VI), consistent with reduction. XANES analysis of sediments supported U(VI) reduction with the precipitation of U(IV). U(VI) reduction activity occurred concurrent with an increase in dissolved organic carbon (DOC) and cell and virus abundance and activity. Metagenome assembled genomes from the microbial community revealed the metabolic potential indicating complex carbon degradation, fermentation, mineralization as well as the potential for anaerobic respiration of nitrate, metal/radionuclides, and sulfate. The virome recovered from the samples indicated a change in viral community in response to nitrate amendments and viral-encoded carbohydrate active enzymes were upregulated indicating a coupled response of both viral and microbial community regulating nitrate stimulated carbon biogeochemical cycling. These data together suggest that the addition of an electron acceptor in to organic carbon reduced sediments stimulates not only microbial but also viral activity leading to upregulation of genes associated with carbon biogeochemical cycling in sedimentary systems. While genes associated with metal oxidation are observed, net reduction of uranium prevails leading to uranium immobilization at low nitrate concentrations. Thus together these data indicate a tipping point whereby the influx of nitrate into the reduced environment can influence uranium mobility in DOC and carbon cycling supporting microbial activity and reducing conditions subsurface systems.
硝酸盐刺激了沉积体系中微生物和病毒的活动以及随后对铀迁移的影响
自然发生的铀(U)的动员已被认为是导致地下含水层地源性铀地下水污染的原因。除了碳酸盐配体络合作用外,硝酸盐还通过氧化还原反应改变铀的溶解度,从而控制铀的迁移率。硝酸盐是一种常见的人为污染物,通常在管理土地上的冲积含水层中以高浓度存在。冲积沉积过程形成了这些含水层,形成了一个岩性不均匀的地下,砂、粉砂和粘土之间有明确的接触。这导致有机碳的沉积和还原金属/放射性核素的积累,包括U(IV),在更细粒度的粉砂和粘土中。在含铀冲积含水层粉砂沉积物中加入高硝酸盐孔隙水,刺激了硝酸盐还原微生物群落,这些微生物群落能够催化U(IV)氧化并将U动员到孔隙水中。然而,来自含水层范围研究的元数据和随后的实验表明,这一结果与浓度有关。低浓度含硝酸盐孔隙水加入富有机质含铀沉积物中,导致溶解U(VI)减少,与还原一致。沉积物的XANES分析支持U(VI)随着U(IV)的沉淀而还原。U(VI)还原活性与溶解有机碳(DOC)、细胞和病毒丰度和活性的增加同时发生。来自微生物群落的宏基因组组装基因组揭示了代谢潜力,表明复杂的碳降解,发酵,矿化以及硝酸盐,金属/放射性核素和硫酸盐的厌氧呼吸潜力。从样品中恢复的病毒组表明,病毒群落对硝酸盐修饰的响应发生了变化,病毒编码的碳水化合物活性酶的表达上调,表明病毒和微生物群落对硝酸盐刺激的碳生物地球化学循环的耦合响应。这些数据共同表明,在有机碳还原沉积物中添加电子受体不仅会刺激微生物活性,还会刺激病毒活性,从而导致沉积系统中与碳生物地球化学循环相关的基因上调。虽然观察到与金属氧化相关的基因,但铀的净还原普遍存在,导致铀在低硝酸盐浓度下固定。因此,这些数据共同表明了一个临界点,即硝酸盐流入还原环境可以影响DOC中铀的流动性和碳循环,支持微生物活动和还原地下系统的条件。
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