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富营养化湖泊沉积物中HS、铁和锰对微生物还原NO-过程的控制

Controls of HS, Fe, and Mn on Microbial NO -Reducing Processes in Sediments of an Eutrophic Lake.

作者信息

Cojean Adeline N Y, Lehmann Moritz F, Robertson Elizabeth K, Thamdrup Bo, Zopfi Jakob

机构信息

Department of Environmental Sciences, Aquatic and Stable Isotope Biogeochemistry, University of Basel, Basel, Switzerland.

Department of Marine Science, University of Gothenburg, Gothenburg, Sweden.

出版信息

Front Microbiol. 2020 Jun 16;11:1158. doi: 10.3389/fmicb.2020.01158. eCollection 2020.

Abstract

Understanding the biogeochemical controls on the partitioning between nitrogen (N) removal through denitrification and anaerobic ammonium oxidation (anammox), and N recycling via dissimilatory nitrate (NO ) reduction to ammonium (DNRA) is crucial for constraining lacustrine N budgets. Besides organic carbon, inorganic compounds may serve as electron donors for NO reduction, yet the significance of lithotrophic NO reduction in the environment is still poorly understood. Conducting incubation experiments with additions of N-labeled compounds and reduced inorganic substrates (HS, Fe, Mn), we assessed the role of alternative electron donors in regulating the partitioning between the different NO -reducing processes in ferruginous surface sediments of Lake Lugano, Switzerland. In sediment slurry incubations without added inorganic substrates, denitrification and DNRA were the dominant NO -reducing pathways, with DNRA contributing between 31 and 46% to the total NO reduction. The contribution of anammox was less than 1%. Denitrification rates were stimulated by low to moderate additions of ferrous iron (Fe ≤ 258 μM) but almost completely suppressed at higher levels (≥1300 μM). Conversely, DNRA was stimulated only at higher Fe concentrations. Dissolved sulfide (HS, i.e., sum of HS, HS and S) concentrations up to ∼80 μM, strongly stimulated denitrification, but did not affect DNRA significantly. At higher HS levels (≥125 μM), both processes were inhibited. We were unable to find clear evidence for Mn-supported lithotrophic NO reduction. However, at high concentrations (∼500 μM), Mn additions inhibited NO reduction, while it did not affect the balance between the two NO reduction pathways. Our results provide experimental evidence for chemolithotrophic denitrification or DNRA with Fe and HS in the Lake Lugano sediments, and demonstrate that all tested potential electron donors, despite the beneficial effect at low concentrations of some of them, can inhibit NO reduction at high concentration levels. Our findings thus imply that the concentration of inorganic electron donors in lake sediments can act as an important regulator of both benthic denitrification and DNRA rates, and suggest that they can exert an important control on the relative partitioning between microbial N removal and N retention in lakes.

摘要

了解生物地球化学对通过反硝化作用去除氮(N)和厌氧氨氧化(anammox)之间分配的控制,以及通过异化硝酸盐(NO)还原为铵(DNRA)实现的氮循环,对于确定湖泊氮收支至关重要。除了有机碳,无机化合物可作为NO还原的电子供体,但环境中无机营养型NO还原的重要性仍知之甚少。通过添加N标记化合物和还原无机底物(HS、Fe、Mn)进行培养实验,我们评估了替代电子供体在调节瑞士卢加诺湖铁质表层沉积物中不同NO还原过程之间分配的作用。在未添加无机底物的沉积物浆液培养中,反硝化作用和DNRA是主要的NO还原途径,DNRA占总NO还原量的31%至46%。厌氧氨氧化的贡献小于1%。低至中等添加量的亚铁(Fe≤258μM)刺激反硝化速率,但在较高水平(≥1300μM)时几乎完全抑制。相反,仅在较高的铁浓度下DNRA受到刺激。高达约80μM的溶解硫化物(HS,即HS、HS和S的总和)浓度强烈刺激反硝化作用,但对DNRA没有显著影响。在较高的HS水平(≥125μM)下,两个过程均受到抑制。我们未能找到明确证据证明锰支持无机营养型NO还原。然而,在高浓度(约500μM)下,添加锰抑制NO还原,而不影响两种NO还原途径之间的平衡。我们的结果为卢加诺湖沉积物中利用Fe和HS进行化学无机营养型反硝化或DNRA提供了实验证据,并表明所有测试的潜在电子供体,尽管其中一些在低浓度时有有益作用,但在高浓度时均可抑制NO还原。因此,我们的研究结果表明,湖泊沉积物中无机电子供体的浓度可作为底栖反硝化作用和DNRA速率的重要调节剂,并表明它们可对湖泊中微生物氮去除和氮保留之间的相对分配施加重要控制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5aa9/7308436/cdba676a3da8/fmicb-11-01158-g001.jpg

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