Multi-isotope (δ 2H, δ 18O, δ 13C-TDIC, δ 18O-TDIC, 87Sr/86Sr) and hydrochemical study on fractured-karstic and detritic shallow aquifers in the Pampean region, Argentina.

Fluxes between fractured-karstified and detritic aquifers are commonly poorly understood in many environments. These two types of aquifers are in contact in the southeastern Pampean region in the Argentine Buenos Aires province, and the aim of this work is to analyze their relationship contributing to improve the hydrological model. A joint application of hydrochemical and multi-isotope (δ 2H, δ 18O, δ 13C-TDIC, δ 18O-TDIC, 87Sr/86Sr) tools was used. TDIC, δ 2H, δ 18O and δ 13C-TDIC allowed differentiating two main end members. Water in the Pampeano aquifer (PA) which is transferred from the fractured-karstic aquifer (F-KA) is characterised by high TDIC around 500-700 mg/L, isotopically depleted in 18O (about -5.5 ‰) and high δ 13C-TDIC (around -10.0 ‰). The other end member is direct recharge water infiltrated into the PA with TDIC ranging from 400 to 500 mg/L, slightly enriched in 18O (δ 18O = -4.8 ‰), and δ 13C-TDIC in the range of soil CO2 as a result of reactions with calcrete concretions (from -20.0 to -9.0 ‰). Dolomite dissolution is the main process controlling the chemistry of the low-mineralized (Mg-Ca-HCO3) waters, whereas high-mineralized (Na-HCO3) waters are strongly influenced by ion-exchange reactions with adsorbed Ca2+ and Mg2+ and by evaporation.

Application of hydrogeochemistry and isotopic characterization for the assessment of recharge in a volcanic aquifer in the eastern region of central Costa Rica.

In the eastern region of central Costa Rica, land use in the sub-basins of the Maravilla-Chiz and Quebrada Honda rivers (47 km2) is dominated by agricultural and livestock production, while groundwater resources constitute the main drinking water supply. This study aimed to (a) evaluate the location of groundwater recharge areas and groundwater flow paths, and (b) provide a characterization of the hydrochemistry and possible anthropic impacts. Groundwater was collected from 20 sites during the dry and rainy seasons and analysed for major ions, water stable isotopes and 222Rn. Approximated recharge areas were estimated through a local altitudinal line based on isotopic compositions in springs. The hydrochemical and isotopic characterization of groundwater showed that the main recharge areas occur in the upper part of the basin, except for springs in the middle part of the basin probably due to a certain hydraulic disconnection from the upper part that facilitates local recharge processes. In the lower basin, groundwater exhibited greater transit times and longer flow paths. Low nitrate, chloride and sulphate concentrations found in groundwater indicate low leaching of fertilizers or urban wastewaters. Our results are focused to improve water resources and agricultural management plans in a dynamic tropical landscape.

Quantification of methane emissions in a Mediterranean landfill (Southern Spain). A combination of flux chambers and geostatistical methods.

In this study, landfill gas emissions from a landfill located in southern Spain were estimated using static surface flux chambers and applying and comparing four geostatistical methods; ordinary kriging, lognormal kriging, intrinsic random functions of order K and indicator kriging. This paper presents the methodology used to calculate methane (and carbon dioxide) emissions from a landfill in southern Spain. Static flux chambers were used to estimate emissions through the sealing layer of a landfill assuming that the geospatial mean best expresses the average value of these emissions. This study considers several geostatistical methods for obtaining the corresponding spatial estimation, using measurements obtained from static flux chambers and finding the best proven results. The most appropriate geostatistical analysis method was found to be indicator kriging and lognormal kriging because of the simplicity of its implementation and the transformation of the flux measurements. Methane surface emissions (100 g·m-2·d-1) and visualization of the hotspots were significant enough to result in the placement of a new cover across the entire landfill. This additional cover had an immediate impact on the effectiveness of the recovery system and increased LFG collection flow rates by 15% with an increase in CH4 concentration in the collected gas from 50% to 60%.

Application of stable isotopes (δ³4S-SO4, δ¹8O-SO4, δ¹5N-NO 3, δ¹8O-NO 3) to determine natural background and contamination sources in the Guadalhorce River Basin (southern Spain).

The integrated use of isotopes (δ(34)S-SO4, δ(18)O-SO4, δ(15)N-NO3, δ(18)O-NO3), taking into account existing hydrogeological knowledge of the study area (mainly hydrochemical), was applied in the Guadalhorce River Basin (southern Spain) to characterise SO4(2-) and NO3(-) sources, and to quantify natural background levels (NBLs) in groundwater bodies. According to Water Framework Directive 2000/60/EC and, more recently, Groundwater Directive 2006/118/EC, it is important to determine NBLs, as their correct assessment is the first, essential step to characterising groundwater bodies, establishing threshold values, assessing chemical status and identifying trends in pollutant concentrations. In many cases, NBLs are high for some parameters and types of groundwater, making it difficult to distinguish clearly between factors of natural or human origin. The main advantages of using stable isotopes in a complex area like the Guadalhorce River Basin that exhibits widely varying hydrogeological and hydrochemical conditions and longstanding anthropogenic influences (mainly agriculture, but also many others) is accurate determination of pollution sources and precise quantification of NBLs. Since chemical analyses only provides the concentration of pollutants in water and not the source, three isotopic sampling campaigns for sulphates (δ(34)S-SO4, δ(18)O-SO4) were carried out, in 2006, 2007 and 2012, and another one was conducted for nitrates (δ(15)N-NO3, δ(18)O-NO3), in 2009, in groundwater bodies in order to trace the origins of each pollutant. The present study identified different pollution sources of dissolved NO3(-) in groundwater using an isotopic composition and quantified the percentage of natural (lithology, chemical and biological processes) and anthropogenic (fertilisers, manure and sewage) SO4(2-) and matched a concentration associated with the percentage in order to determine the NBLs in the basin.

Determination of background levels on water quality of groundwater bodies: a methodological proposal applied to a Mediterranean River basin (Guadalhorce River, Málaga, southern Spain).

Determine background levels are a key element in the further characterisation of groundwater bodies, according to Water Framework Directive 2000/60/EC and, more specifically, Groundwater Directive 2006/118/EC. In many cases, these levels present very high values for some parameters and types of groundwater, which is significant for their correct estimation as a prior step to establishing thresholds, assessing the status of water bodies and subsequently identifying contaminant patterns. The Guadalhorce River basin presents widely varying hydrogeological and hydrochemical conditions. Therefore, its background levels are the result of the many factors represented in the natural chemical composition of water bodies in this basin. The question of determining background levels under objective criteria is generally addressed as a statistical problem, arising from the many aspects involved in its calculation. In the present study, we outline the advantages of applying two statistical techniques applied specifically for this purpose: (1) the iterative 2σ technique and (2) the distribution function, and examine whether the conclusions reached by these techniques are similar or whether they differ considerably. In addition, we identify the specific characteristics of each approach and the circumstances under which they should be used.