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Nadler, A., Magaritz, M., & Mazor, E. (1980). Chemical reactions of sea water with rocks and freshwater: Experimental and field observations on brackish waters in Israel. Geochimica et Cosmochimica Acta, 44(6), 879–886.
Abstract: Four major processes are observed to take place in the coastal aquifer of Israel, detectable even in the short times of water contact with the carbonate-containing host rocks. Three are chemical reactions, Ca2+-Mg2+ exchange, Na+-Ca2+ or Na+-Mg2+ base exchange, SO2−4 reduction and the fourth is dilution by freshwater. These reactions and their effects on the chemical composition of the waters were demonstrated experimentally. The range of chemical changes observed in the laboratory experiments overlap the range of the studied natural waters. This indicates that simulation of geologically long-term rock-water interaction could be achieved in laboratory experiments even at low temperatures.
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Houben, G. (2018). Annotated translation of “Die Wasserversorgung einiger Nordseebäder [The water supply of some North Sea spas]” by Alexander Herzberg (1901). Hydrogeology Journal, 26(6), 1789–1799.
Abstract: The publication “The water supply of some North Sea spas” by Alexander Herzberg in 1901 is a cornerstone of coastal groundwater research. It was fundamental to the development of the Ghijben-Herzberg principle, which describes the hydrostatic equilibrium between fresh and saline groundwater. Due to its age and the language barrier, the paper is often cited but probably rarely read. Therefore, the original paper has been translated from German into English, accompanied by an introduction and notes explaining the historical context.
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Vengosh, A., Spivack, A. J., Artzi, Y., & Ayalon, A. (1999). Geochemical and boron, strontium, and oxygen isotopic constraints on the origin of the salinity in groundwater from the Mediterranean coast of Israel. Water Resources Research, 35(6), 1877–1894.
Abstract: In order to identify the origin of the salinity and formation of saline plumes in the central part of the Mediterranean coastal aquifer of Israel, we determined the elemental and boron, strontium, and oxygen isotopic compositions of fresh and brackish groundwater (C1 up to 1500 mg/L). We distinguish between two key anthropogenic sources: (1) sewage effluents used for irrigation with high Na/C1, SO4/C1, and B/C1 ratios and low Br/C1 ratios relative to seawater ratios, low ;5•B values (0-10%o) and high ;5•80 values (>-4%0); and (2) imported water from the Sea of Galilee that is artificially
recharged tothe aquifer with high Br/C1 (3 x 10 -3) and ;5•80 values (-1%o) and a low 87Sr/86Sr ratio of 0.70753. The brackish groundwater from the saline plumes have relatively low Na/C1 ratios (0.5-0.8) and high Ca/Mg, Mg/C1, and Ca/(SO 4 q- HCO3) (> l) ratios relative to seawater ratios; marine SO4/C1 and Br/C1 ratios;5•B values of 24.8-49.9%0; 18 87 86 ;50 of -2.95%0 to -4.73%0; and Sr/ Sr ratios of 0.708275-0.708532. The composition of most of the investigated groundwater from the saline plumes differs from those of the 87 86 anthropogenic sources, imported water, fresh uncontaminated groundwater (Sr/ Sr of 0.70866, ;5•B of 20-30%o), and saline water from the adjacent Eocene aquitard. Only in ß 18 areas of artificial recharge does local groundwater have high Br/C1 and ;50 values that are typical to the Sea of Galilee. The linear relationships between chloride and most of the ions, including Band Sr, the relatively high ;5•B (>30%0) and low ;5•80 (<-4%0) values, and the chemical signature of the saline plumes (e.g., marine Br/C1 and SO4/C1 ratios), suggest that (1) mixing processes control the chemical composition of the brackish water within the aquifer, and (2) the saline postulated end-member has a chemical composition that resembles modified seawater with a marine and higher ;5•B values, and a 87Sr/86Sr ratio of <0.7083. We propose that most of the salinization phenomena and the formation of saline plumes in the inner parts of the coastal aquifer are derived from upconing of underlying natural saline water bodies and enhanced by overexploitation and draw-down of the overlying fresh groundwater.
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Han, D., & Currell, M. J. (2018). Delineating multiple salinization processes in a coastal plain aquifer, northern China: hydrochemical and isotopic evidence. Hydrology and Earth System Sciences, 22(6), 3473–3491.
Abstract: Groundwater is an important water resource for agricultural irrigation and urban and industrial utilization in the coastal regions of northern China. In the past 5 decades, coastal groundwater salinization in the Yang–Dai river plain has become increasingly serious under the influence of anthropogenic activities and climatic change. It is pivotal for the scientific management of coastal water resources to accurately understand groundwater salinization processes and their causative factors. Hydrochemical (major ion and trace element) and stable isotopic (δ18O and δ2H) analysis of different water bodies (surface water, groundwater, geothermal water and seawater) were conducted to improve understanding of groundwater salinization processes in the plain's Quaternary aquifer. Saltwater intrusion due to intensive groundwater pumping is a major process, either by vertical infiltration along riverbeds which convey saline surface water inland, and/or direct subsurface lateral inflow. Trends in salinity with depth indicate that the former may be more important than previously assumed. The proportion of seawater in groundwater is estimated to have reached up to 13 % in shallow groundwater of a local well field. End-member mixing calculations also indicate that the geothermal water with high total dissolved solids (up to 10.6 g L−1) with depleted stable isotope compositions and elevated strontium concentrations (> 10 mg L−1) also mixes locally with water in the overlying Quaternary aquifers. This is particularly evident in samples with elevated Sr ∕ Cl ratios (> 0.005 mass ratio). Deterioration of groundwater quality by salinization is also clearly exacerbated by anthropogenic pollution. Nitrate contamination via intrusion of heavily polluted marine water is evident locally (e.g., in the Zaoyuan well field); however, more widespread nitrate contamination due to other local sources such as fertilizers and/or domestic wastewater is evident on the basis of NO3 ∕ Cl ratios. This study provides an example of how multiple geochemical indicators can delineate different salinization processes and guide future water management practices in a densely populated water-stressed coastal region.
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Post, V. E. A., Houben, G. J., & van Engelen, J. (2018). What is the Ghijben-Herzberg principle and who formulated it? Hydrogeology Journal, 26(6), 1801–1807.
Abstract: It has been suggested in a number of historical notes that it was neither Willem Badon Ghijben nor Alexander Herzberg who formulated the famous principle now carrying their name, which relates the water-table elevation to the depth of the freshwater saltwater interface in coastal aquifers. In this paper, a systematic review of the literature pre-dating the publication of their work is presented. The aim is to establish to what extent these previous works captured the essence of the Ghijben-Herzberg principle, that is, the combination of a correct conceptual model of the hydrogeological conditions with a quantitative relationship. It was found that references to coastal fresh groundwater reserves can be traced back to Roman times, while the earliest detailed descriptions of a freshwater lens that could be found dates from the eighteenth century. The correct understanding of the hydrostatic equilibrium between fresh and salt groundwater is evident in works from the early nineteenth century. However, it was Badon Ghijben and Herzberg who combined this with the correct understanding of the groundwater conditions of a freshwater lens. It was further found that Herzberg had already recorded his findings in 1888 in a hand-written report, confirming speculation that such a report might exist.
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