scholarly journals Using hydraulic head, chloride and electrical conductivity data to distinguish between mountain-front and mountain-block recharge to basin aquifers

2017 ◽  
Author(s):  
Etienne Bresciani ◽  
Roger H. Cranswick ◽  
Eddie W. Banks ◽  
Jordi Batlle-Aguilar ◽  
Peter G. Cook ◽  
...  

Abstract. Numerous basin aquifers in arid and semi-arid regions of the world derive a significant portion of their recharge from adjacent mountains. Recharge can effectively occur through either stream infiltration in the mountain front zone (mountain-front recharge, MFR) or subsurface flow from the mountain (mountain-block recharge, MBR). While a thorough understanding of the recharge mechanisms is critical for water resource management, distinguishing between MFR and MBR is typically difficult. Here we present a relatively simple approach that uses hydraulic head, chloride and electrical conductivity data to distinguish between MFR and MBR. These types of data are inexpensive to measure, and in many cases are readily available from hydrogeological databases. In principle, hydraulic head can inform on groundwater flow directions and stream-aquifer interactions, while chloride can help to distinguish between different groundwater pathways if the sources have distinct concentrations. Electrical conductivity values can be converted to chloride concentrations using an empirical relationship, and hence can be used in a similar manner to chloride, thereby significantly increasing the data set. The practical feasibility and effectiveness of this approach are tested through the case study of the Adelaide Plains basin, South Australia, for which a wealth of historical groundwater level, chloride and electrical conductivity data is available. Hydraulic head data suggest that streams are gaining in the adjacent Mount Lofty Ranges and losing when entering the basin. They also indicate that not only the Quaternary sediments but also the underlying Tertiary sediments receive significant recharge from stream leakage in the mountain front zone. Chloride data also reveal clear spatial patterns suggesting that MFR dominates recharge of the low salinity groundwater found in the basin. This interpretation is further supported by stream water chloride analysis. This study demonstrates that both hydraulic head and chloride data can be effectively used to distinguish between MFR and MBR.

2018 ◽  
Vol 22 (2) ◽  
pp. 1629-1648 ◽  
Author(s):  
Etienne Bresciani ◽  
Roger H. Cranswick ◽  
Eddie W. Banks ◽  
Jordi Batlle-Aguilar ◽  
Peter G. Cook ◽  
...  

Abstract. Numerous basin aquifers in arid and semi-arid regions of the world derive a significant portion of their recharge from adjacent mountains. Such recharge can effectively occur through either stream infiltration in the mountain-front zone (mountain-front recharge, MFR) or subsurface flow from the mountain (mountain-block recharge, MBR). While a thorough understanding of recharge mechanisms is critical for conceptualizing and managing groundwater systems, distinguishing between MFR and MBR is difficult. We present an approach that uses hydraulic head, chloride and electrical conductivity (EC) data to distinguish between MFR and MBR. These variables are inexpensive to measure, and may be readily available from hydrogeological databases in many cases. Hydraulic heads can provide information on groundwater flow directions and stream–aquifer interactions, while chloride concentrations and EC values can be used to distinguish between different water sources if these have a distinct signature. Such information can provide evidence for the occurrence or absence of MFR and MBR. This approach is tested through application to the Adelaide Plains basin, South Australia. The recharge mechanisms of this basin have long been debated, in part due to difficulties in understanding the hydraulic role of faults. Both hydraulic head and chloride (equivalently, EC) data consistently suggest that streams are gaining in the adjacent Mount Lofty Ranges and losing when entering the basin. Moreover, the data indicate that not only the Quaternary aquifers but also the deeper Tertiary aquifers are recharged through MFR and not MBR. It is expected that this finding will have a significant impact on the management of water resources in the region. This study demonstrates the relevance of using hydraulic head, chloride and EC data to distinguish between MFR and MBR.


1994 ◽  
Vol 367 ◽  
Author(s):  
Y. Carolina Araujo ◽  
Pedro G. Toledo ◽  
Hada Y. Gonzalez

AbstractTransport properties of natural porous media have been observed to obey scaling laws in the wetting phase saturation. Previous work relates power-law behavior at low wetting phase saturations, i.e., at high capillary pressures, to the thin-film physics of the wetting phase and the fractal character of the pore space of porous media. Here, we present recent combined porousplate capillary pressure and electrical conductivity data of Berea sandstone at low saturations that lend support to the scaling laws. Power law is interpreted in terms of the exponent m in the relation of surface forces and film thickness and the fractal dimension D of the interface between pore space and solid matrix. Simple determination of D from capillary pressure and m from electrical conductivity data can be used to rapidly determine wetting phase relative permeability and capillary dispersion coefficient at low wetting phase saturations.


1996 ◽  
Vol 457 ◽  
Author(s):  
O. Porat ◽  
H. L. Tuller ◽  
E. B. Lavik ◽  
Y.-M. Chiang

ABSTRACTOxygen nonstoichiometry measurements in nanocrystalline ceria, x in CeO2-x, were performed using coulometric titration. The measurements reveal large apparent deviations from stoichiometry, of the order of 10−3 − 10−4 at T = 405 − 455 °C and Po2 = 0.21 − 10−5 atm, as compared to levels of ∼10−9 for coarsened materials under the same conditions. The level of nonstoichiometry is, however, larger then expected from previous electrical conductivity data of nanocrystalline ceria. In addition, x ∝ Po2−½ while Σ ∝po2−1/6. The observed dependence of x(Po2, T) can be explained by either the formation of neutral oxygen vacancies at or near the interface, or by surface adsorption.


2003 ◽  
Vol 102 (1-3) ◽  
pp. 83-91 ◽  
Author(s):  
M. Prego ◽  
E. Rilo ◽  
E. Carballo ◽  
C. Franjo ◽  
E. Jiménez ◽  
...  

2017 ◽  
Vol 31 (9) ◽  
pp. 1702-1718 ◽  
Author(s):  
Marie-Paule Bonnet ◽  
Sébastien Pinel ◽  
Jérémie Garnier ◽  
Julie Bois ◽  
Géraldo Resende Boaventura ◽  
...  

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