Radionuclides as natural tracers of the interaction between groundwater and surface water in the River Andarax, Spain.

J Environ Radioact

LARUEX, Environmental Radioactivity Laboratory, Dpt. Applied Physics, Faculty of Veterinary Sciences, Avda. Universidad, s/n, 10003, Cáceres, Spain.

Published: December 2017

The identification of specific aquifers that supply water to river systems is fundamental to understanding the dynamics of the rivers' hydrochemistry, particularly in arid and semiarid environments where river flow may be discontinuous. There are multiple methods to identify the source of river water. In this study of the River Andarax, in the Southeast of Spain, an analysis of natural tracers (physico-chemical parameters, uranium, radium and radon) in surface water and groundwater indicates that chemical parameters and uranium clearly identify the areas where there is groundwater-surface water interaction. The concentration of uranium found in the river defines two areas: the headwaters with U concentrations of 2 μg L and the lower reaches, with U of 6 μg L. Furthermore, variation in the U/U isotopic ratio allowed us to detect the influence that groundwater from the carbonate aquifer has on surface water in the headwaters of the river, where the saline content is lower and the water has a calcium bicarbonate facies. The concentration of Ra and Rn are low in the surface waters: <1.6 × 10 μg L and <5.1 × 10 μg L, respectively. There is a slight increase in the lower reaches where the water has a permanent flow, greater salinity and a calcium-magnesium-sulphate facies. All this is favoured by the influence of groundwater from the detritic aquifer on the surface waters. The results of this study indicate the utility in the use of physico-chemical and radiological data conjointly as tracers of groundwater-surface water interaction in semiarid areas where the lithology of aquifers is diverse (carbonate and detritic) and where evaporitic rocks are present.

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.jenvrad.2017.09.015DOI Listing

Publication Analysis

Top Keywords

surface water
12
natural tracers
8
water river
8
river andarax
8
parameters uranium
8
water
7
river
7
radionuclides natural
4
tracers interaction
4
interaction groundwater
4

Similar Publications

Soliton Dynamics over a Disordered Topography.

Phys Rev Lett

December 2024

MSC, CNRS, Université Paris Cité, UMR 7057, F-75013 Paris, France.

We report on the dynamics of a soliton propagating on the surface of a fluid in a 4-m-long canal with a random or periodic bottom topography. Using a full space-and-time resolved wave field measurement, we evidence, for the first time experimentally, how the soliton is affected by the disorder, in the context of Anderson localization, and how localization depends on nonlinearity. For weak soliton amplitudes, the localization length is found in quantitative agreement with a linear shallow-water theory.

View Article and Find Full Text PDF

Dental ultrasonic scalers are commonly employed in periodontal treatment; however, their ability to roughen tooth surfaces is a worry since roughness may increase plaque production, a key cause of periodontal disease. This research studied the influence of a piezoelectric ultrasonic scaler on the roughness of two distinct flowable composite filling materials. To do this, 10 disc-shaped samples were generated from each of the two flowable composite materials.

View Article and Find Full Text PDF

Spontaneous adsorption of iridium chloride complex on oxychloride photocatalysts provides efficient and durable reaction site for water oxidation.

Chem Commun (Camb)

January 2025

Department of Energy and Hydrocarbon Chemistry, Graduate School of Engineering, Kyoto University, Nishikyo-ku, Kyoto 615-8510, Japan.

The visible-light-driven O evolution on oxychloride photocatalysts, such as BiNbOCl, was significantly enhanced by stirring in an aqueous solution containing IrCl in the dark. Various characterizations indicated that highly dispersed IrOHCl-like species spontaneously formed on the oxychloride surface, serving as effective and stable cocatalysts for enhancing O evolution.

View Article and Find Full Text PDF

Comparison of Hydrogen Bonded Organic Framework with Reduced Graphene Oxide-Pd Based Nanocatalyst: Which One Is More Efficient for Entrapment of Nitrophenol Pollutants?

Langmuir

January 2025

Prof. Rashidi Laboratory of Organometallic Chemistry & Material Chemistry, Department of Chemistry, College of Science, Shiraz University, Shiraz, 7194684795, Iran.

In this study, a Pd nanoparticles@hydrogen-bonded organic framework (Pd NPs@HOF) thin film was fabricated at the toluene-water interface. The HOF was formed through the interaction of trimesic acid (TMA) and melamine (Mel) in the water phase, while Pd(0) was produced from the reduction of [PdCl(cod)] in the organic phase. The as-synthesized Pd NPs@HOF thin film was demonstrated to be an effective catalyst for the selective reduction of -nitrophenol and -nitrophenol to -aminophenol and -aminophenol.

View Article and Find Full Text PDF

An understanding of proton transfer and migration at the surfaces of solid metal oxides and related molecular polyoxometalates (POMs) and metal alkoxides is crucial for the development of reactivity involving protonation or the absorption/binding of water. In this work, the hydrolysis of alkoxido Ti- and Sn-substituted Lindqvist [(MeO)MWO] (M = Ti, ; M = Sn, ) and Keggin [(MeO)MPWO] (M = Ti, ; M = Sn, ) type polyoxometalates (POMs) to hydroxido derivatives and subsequent condensation to μ-oxido species has been investigated in detail to provide insight into proton transfer reactions in these molecular metal oxide systems. Solution NMR studies revealed the dependence of reactions not only on the nature of the heteroatom (Ti or Sn) but also on the type of lacunary (W or PW) POM and also on the solvent (MeCN or DMSO).

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!