Spatial and temporal variations in groundwater nitrate at an intensive dairy farm in south-east Ireland: Insights from stable isotope data

Achievement of at least “good ecological status” in all waterbodies under the EU Water Framework Directive by 2015 will in some cases be a challenge. The twin challenge is to manage expectations of policy makers for such waterbodies as to a realistic length of time required for improvement in water quality. Hence, understanding the source, transformation processes and residence time of nitrate in a hydrological system is an essential part of meeting such challenges. On a dairy farm with 24 shallow groundwater wells, the dual isotopic composition of nitrate (δ¹⁵N and δ¹⁸O) was used to clarify nitrate sources, to assess spatial and temporal variability in nitrate concentrations and to determine if and where denitrification was occurring. Vertical travel time was estimated to correlate nitrate concentrations with management practices. Organically derived nitrogen was the predominant source contributing to groundwater nitrate concentrations. Denitrification was identified as prevalent within specific regions of the study site. The distinct low temporal variability in the isotopic data suggests constancy among nitrate sources and processes over time across the study site. Vertical travel times of up to 3 years were estimated on site indicating the influence of recent management practices on nitrate concentrations. Very slow horizontal migration of groundwater (decades) indicates a legacy of older management practices. Stable isotope techniques, together with an understanding of time lag, provide an extra mechanism to test the efficacy of monitoring and mitigation programmes.     

The water supply footprint (WSF): a strategic planning tool for sustainable regional and local water supplies

This paper introduces a new methodological approach of the ecological footprint explicitly addressing the sustainability of water supplies, which we call the water supply footprint (WSF). The WSF calculates the catchment area or water supply hinterland of a certain society and can serve as a strategic planning tool for local or regional water supplies linking the water demand with the water supply in a water supply footprint matrix. Based on regional water balances it estimates how much water can be appropriated for human use in an environmentally sustainable way.The proposed method is tested on the South East Queensland water supply in Australia, an area where water use restrictions are regularly imposed on the population. Applying the proposed method indicates that supply shortages may be avoided by considerably changing the organisation of water supply, thereby reducing and possibly even avoiding the necessity for large-scale supply side measures like additional sweet water reservoirs or desalination plants. In that way it is demonstrated that the WSF method is applicable at an early and strategic stage of water supply planning.     

土著微生物修复城市小型湖泊实验研究

利用生物制剂及生物修复技术对鞍山市英泽湖进行了净化治理.研究结果表明,经过8～30 d的生物净化,该湖水中的COD、植物营养元素浓度及浊度都有了大幅度的下降.其中COD降至20 mg/L以下,去除率达到70%以上;氨氮降至0.2 mg/L以下,去除率达97%;总磷降低至0.02 mg/L以下,去除率达到60%以上;浊度...     

流域水污染防治绩效评估体系研究

以环境绩效评估为基础,从总量削减、水环境质量保护、公众参与、环境治理4个方面选择指标,采用层次分析法进行水污染防治绩效评估.结果表明,赣江流域水污染防治效果明显,水环境质量呈逐年变好趋势;从环境管理来看,情况有所改善,但还存在一些问题,环保投资指数成为影响水污染防治效果的主要控制因子.     

工业废水中钡的排放限值研究

在查阅大量文献资料基础上,总结了环境中钡的来源和特性,采用电感耦合等离子原子发射光谱方法测定地表水及稀土废水中的钡元素含量.对仪器的工作参数和被测元素的分析谱线进行了优化和选择,结合钡的化学毒性,提出了废水中钡的标准是5mg/L的建议.     

火焰原子吸收法测定水中的总铬

用火焰原子吸收光谱法测定水中总铬,乙炔流量100L/h、燃烧头高度为9mm、狭缝宽度0.2 nm时,灵敏度和重现性最好.1 mg/L铬溶液中盐酸含量5％、氯化铵含量0.5％时,吸光度较高,相对标准偏差最低.该方法操作简便,灵敏度好,精确度和准确度高,便于推广,适合水中总铬的测定.     

石墨炉原子吸收法测定水中铊的方法改进

采用石墨炉原子吸收法测定水中铊，对样品前处理的多个细节进行改进，使前处理过程耗时缩短，回收率提高。试验表明，方法在0μg/L ～50．0μg/L范围内线性良好，相关系数r为0．9995；检出限为2．0μg/L，取样量为500 mL，富集50倍时，方法检出限为0．04μg/L；实际水样测定结果的 RSD 为4．9％～8．4％；实际样品的加标回收率为94．0％～102％。     

气相色谱-高分辨双聚焦磁质谱测定水中超痕量多氯萘

采用固相萃取法处理水样，气相色谱-高分辨双聚焦磁质谱法测定水中超痕量多氯萘，同位素内标法定量，并对样品前处理条件和仪器条件进行优化。试验表明：方法在0．500 ng/L～500 ng/L范围内线性良好；当取样体积为1 L时，方法检出限为0．005 ng/L～0．01 ng/L；对实际水样进行2个质量浓度水平的加标回收试验，平行测定6次的 RSD为2．7％～8．7％，回收率为70．2％～110％。方法适用性试验表明，水样中复杂的基质对测定无影响。     

Numerical simulation of water curtain application for ammonia release dispersion

Using water curtain system to forced mitigate ammonia vapor cloud has been proven to be an effective measure. Currently, no engineering guidelines for designing an effective water curtain system are available, due to lack of understanding of complex interactions between ammonia vapor cloud and water droplets, especially the understanding of ammonia absorption into water droplets. This paper presents numerical calculations to reproduce the continuous ammonia release dispersion with and without the mitigating influence of a downwind water curtain using computational fluid dynamic (CFD) software ANSYS Fluent 14.0. The turbulence models k–ɛ and RNG were used to simulate the ammonia cloud dispersion without downwind water curtain. The simulated results were compared with literature using the statistical performance indicators. The RNG model represents better agreement with the experimental data and the k–ɛ model generates a slightly lesser result. The RNG model coupled with Lagrangian discrete phase model (DPM) was used to simulate the dilution effectiveness of the water curtain system. The ammonia absorption was taken into account by means of user-defined functions (UDF). The simulated effectiveness of water curtains has good agreements with the experimental results. The effectiveness of water mitigation system with and without the ammonia absorption was compared. The results display that the effectiveness mainly depends on the strong air entrainment enhanced by water droplets movement and the ammonia absorption also enhances the effectiveness of water curtain mitigation system. The study indicates that the CFD code can be satisfactorily applied in design criteria for an effective mitigation system.     

水环境中26种类固醇激素的分析方法研究

建立了固相萃取-超高效液相-串联质谱法同时测定水环境中26种类固醇激素的分析方法。明确了取样体积为500 m L,Cleanert PEP为富集柱,乙酸乙酯为洗脱剂,甲醇为溶剂进行提取操作。选择了正离子模式,以0. 1%甲酸/甲醇-水为流动相,负离子模式以0. 1%氨水/乙腈-水为流动相,试样经AcquityTMUPLC BEH C18色谱柱分离后,选用质谱检测模式进行定性、定量分析。通过方法验证,26种类固醇激素的方法检出限为0. 3～1. 5 ng/L,测定下限为1. 2～6. 0 ng/L,代表性样品测定结果的相对标准偏差为2. 6%～13. 7%(n=6),加标回收率为71. 2%～121%。该方法操作便捷,灵敏度高,精密度和准确度良好,可适用于水环境中多种痕量、超痕量类固醇激素的定性定量分析。