15N示踪在人工湿地土壤氮循环过程估算中的应用

IF 11.4 1区 环境科学与生态学 Q1 ENGINEERING, ENVIRONMENTAL
M.M.R. Jahangir , O. Fenton , R. Carolan , R. Harrington , P. Johnston , M. Zaman , K.G. Richards , C. Müller
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引用次数: 13

摘要

综合人工湿地(ICW)区域技术,用于衰减来自点源或扩散源的水中的有机碳(C)、氮(N)、磷(P)和硫(S)等污染物。目前,关于ICW床土壤中总氮转化率导致活性氮向环境损失的知识缺乏。此外,为了可持续地利用ICW去除废水处理中的过量氮,需要对这些过程的动力学进行深入研究。采用15N示踪法定量分析了地表流ICW床上两个土壤深度(0-15 cm和30-45 cm)的总N转化过程。ICW位于爱尔兰东南部沃特福德的Dunhill村,接收500人等量的含有大量有机污染物的废水(每年平均C、N、P和S含量分别为240、60、5和73 mg L - 1)。2014年12月,从这些深度取出土壤,在实验室厌氧培养,15N标记铵(NH4+)或硝酸盐(NO3 -),在平行设置中分别标记14NH415NO3和15NH414NO3,富集至50 atm% 15N。结果表明,在两种土壤深度,NO3−产生速率都较小,这可能是由于反硝化或异效NO3−还原成铵(DNRA)导致的NO3−还原量较低。然而,尽管低,DNRA率大于反硝化率。有机N直接转化为NO3−,而不矿化为NH4+,是NO3−生产的主要途径,占NO3−总产量的28-33%。该过程对总氮矿化的相对贡献在深度1处可忽略不计(0.01%),而在深度2处占主导地位(99.7%)。总NO3 -产生量对总NH4+和NO3 -固定化的影响非常小(<0.50%),表明ICW土壤不是NO3 -的来源。尽管两层均存在较大的氮固定化潜力,但相对于总氮转化,深度2(约2.2)的氮固定化高于深度1(约1.5)。NH4+在30 ~ 45 cm处解吸速率较高。然而,固定性和不稳定性有机氮库的固定性较高。NH4+过程的矿化和固定化表明,顽固性有机氮是ICW土壤的主要来源,而活性有机氮相对较少。N2O产源解析表明,N2O产源主要为反硝化作用(约92.5%),其次为异养硝化作用(约5.5%)、共反硝化作用(约1.90%)和硝化作用(0.20%)。这些结果表明,应用详细的15N示踪方法可以深入了解基于生态系统的活性N丰度的潜在过程。本研究的一个关键发现是,研究的两个ICW层都具有大N固定的特征,这限制了NO3 -的产生和进一步的气态N损失。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Application of 15N tracing for estimating nitrogen cycle processes in soils of a constructed wetland

Integrated Constructed Wetlands (ICW) area technology for the attenuation of contaminants such as organic carbon (C), nitrogen (N), phosphorous (P) and sulphur (S) in water coming from point or diffuse sources. Currently there is a lack of knowledge on the rates of gross N transformations in soils of the ICW bed leading to losses of reactive N to the environment. In addition, the kinetics of these processes need to be studied thoroughly for the sustainable use of ICW for removal of excessive N in the treatment of waste waters. Gross N transformation processes were quantified at two soil depths (0–15 and 30–45 cm) in the bed of a surface flow ICW using a 15N tracing approach. The ICW, located in Dunhill village at Waterford in Southeastern Ireland, receives 500 person equivalent waste waters containing large quantities of organic pollutants (ca. mean annual C, N, P and S contents of 240, 60, 5 and 73 mg L−1). Soil was removed from these depths in December 2014 and incubated anaerobically in the laboratory, with either 15N labeled ammonium (NH4+) or nitrate (NO3), differentially labeled with 14NH415NO3 and 15NH414NO3 in parallel setups, enriched to 50 atm% 15N. Results showed that at both soil depths, NO3 production rates were small, which may have resulted in lower NO3 reduction by either denitrification or dissimilatory NO3 reduction to ammonium (DNRA). However, despite being low, the DNRA rates were greater than denitrification rates. Direct transformation of organic N to NO3, without mineralization to NH4+, was a prevalent pathway of NO3 production accounting for 28–33% of the total NO3 production. Relative contribution of this process to the total N mineralization was negligible at depth 1 (0.01%) but dominant at depth 2 (99.7%). Total NO3production to total immobilization of NH4+ and NO3 was very small (<0.50%) suggesting that ICW soils are not a source of NO3. Despite a large potential of N immobilization existed at both the layers, relative N immobilization to the total N conversion was higher at depth 2 (ca. 2.2) than at depth 1 (ca. 1.5). The NH4+ desorption rate at 30–45 cm was high. However, immobilization in the recalcitrant and labile organic N pools was higher. Mineralization and immobilization of NH4+ processes showed that recalcitrant organic N was the predominant source in ICW soils whereas the labile organic N was comparatively small. Source apportionment of N2O production showed that the majority of the N2O produced through denitrification (ca. 92.5%) followed by heterotrophic nitrification (ca. 5.5%), co-denitrification (ca. 1.90%) and nitrification (0.20%). These results revealed that application of a detailed 15N tracing method can provide insights on the underlying processes of ecosystem based abundances of reactive N. A key finding of this study was that both investigated ICW layers were characterised by large N immobilization which restricts production of NO3 and further gaseous N losses.

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来源期刊
Water Research
Water Research 环境科学-工程:环境
CiteScore
20.80
自引率
9.40%
发文量
1307
审稿时长
38 days
期刊介绍: Water Research, along with its open access companion journal Water Research X, serves as a platform for publishing original research papers covering various aspects of the science and technology related to the anthropogenic water cycle, water quality, and its management worldwide. The audience targeted by the journal comprises biologists, chemical engineers, chemists, civil engineers, environmental engineers, limnologists, and microbiologists. The scope of the journal include: •Treatment processes for water and wastewaters (municipal, agricultural, industrial, and on-site treatment), including resource recovery and residuals management; •Urban hydrology including sewer systems, stormwater management, and green infrastructure; •Drinking water treatment and distribution; •Potable and non-potable water reuse; •Sanitation, public health, and risk assessment; •Anaerobic digestion, solid and hazardous waste management, including source characterization and the effects and control of leachates and gaseous emissions; •Contaminants (chemical, microbial, anthropogenic particles such as nanoparticles or microplastics) and related water quality sensing, monitoring, fate, and assessment; •Anthropogenic impacts on inland, tidal, coastal and urban waters, focusing on surface and ground waters, and point and non-point sources of pollution; •Environmental restoration, linked to surface water, groundwater and groundwater remediation; •Analysis of the interfaces between sediments and water, and between water and atmosphere, focusing specifically on anthropogenic impacts; •Mathematical modelling, systems analysis, machine learning, and beneficial use of big data related to the anthropogenic water cycle; •Socio-economic, policy, and regulations studies.
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