Abstract
Luxor, the modern Egyptian city that occupies the site of ancient Thebes, is famed for its magnificent ancient monuments. Since 1967, the Aswan high dam has prevented the annual flooding of the Nile River, resulting in excessive salt accumulation on the Nile floodplains and on exposed monument surfaces. In addition, the expansion of agricultural land within the Luxor study area has resulted in increased salinity and groundwater level. These conditions accelerate the degradation of buried and exposed monuments that were fairly well preserved in the past. To mitigate this problem, it is necessary to first understand the near-surface setting and the groundwater conditions of the Luxor area. A geophysical investigation was carried out using resistivity and electromagnetic surveys. In addition, a chemical analysis was conducted of some surface water samples collected from canals and the sacred lake of Memnon Temple. Based on the results of the geophysical surveys and the chemical analysis of the water samples, the shallow subsurface was characterized into four geoelecterical units. Groundwater flow directions were determined to be from the central area to the west, causing a rise in the groundwater levels and groundwater salinity in the area of monuments.
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Introduction
Luxor, Egypt, occupies the site ancient Thebes, which was known for its buildings and many large gates. The west bank of Luxor (Fig. 1) contains more than 30 known limestone temples, most of them built by the rulers of the New Kingdom (1549–1069 BC). Both buried and exposed archeological features are affected by the high level of saline groundwater at the west bank of Luxor area since the construction of Aswan high dam and the resultant expansion of agricultural lands around the temples’ area. Saline groundwater is transported into the monuments’ foundations through underlying soil by means of capillary rise. When those saline waters evaporate, residual salts accumulate on the surface and within the pore spaces of the foundations. The pressure developed during the crystallization and hydration of the residual salts exfoliates the outer layers of the foundations’ stone, increasing their susceptibility to erosion by wind and other physical processes (Rodriguez-Navarro and Doehne 1999). Figure 2 shows an example of the monuments’ degradation at Habu Temple in the west bank of Luxor.
Geophysical methods have been widely applied to groundwater exploration (e.g., Asfahani 2007; Ismail 2003; Albouy et al. 2001). Asfahani (2007) employed vertical electrical sounding (VES) at the Khanasser Valley (Syria) and successfully identified the nature and geometry of a deep aquifer. Ismail (2003) conducted a study to mitigate the degradation of monuments on the east bank of Luxor, employing VES and seismic surveys to characterize the hydrostratigraphy of the shallow subsurface. Albouy et al. (2001) examined the merits of using VES and transient electromagnetic (TEM) methods for coastal groundwater exploration, north of Biarritz and at two selected sites at the flanks of le Piton de la Fournaise, France. Those scientists showed that the joint inversion of VES and TEM data are an efficient tool to resolve the ambiguity of each measurement method alone, especially in the absence of supportive geological information, such as well-log data.
The TEM method is an electromagnetic induction technique by which the response of the earth to an electromagnetic impulse is measured in the time domain. The VES method uses direct current to measure the resistance of the subsurface using grounded steel electrodes. Although electrical resistivity and electromagnetic techniques measure the same physical property, soil resistivity, the techniques are sensitive to different characteristics (Gomez-Trevino and Edwards 1983; Raiche et al. 1985). Well-resolved electrical resistivity data obtained using the VES method are the product of layer resistivity and layer thickness (Fitterman et al. 1988). Such data do not provide good independent estimates of layer resistivity and layer thickness. In contrast, electromagnetic methods are good for establishing the thicknesses of layers but not their resistivity values (Fitterman et al. 1988). The combined inversion of TEM and VES data constrains the resistivity-depth geophysical model, and reduces ambiguities in the interpretation of the measurements (Sasaki 1989; Sandberg 1993; Albouy et al. 2001).
In this study, a large-scale geophysical survey was conducted and chemical analysis performed of surface water samples at the west bank of the Nile River (west Luxor area) to characterize the near subsurface hydrogeologic setting and to identify the sources responsible for increasing the salinity of groundwater. The geophysical survey is in the form of integrated TEM and VES measurements. The groundwater analysis included chemical analysis of six surface samples collected from the areas adjacent to the degraded monuments. The results of this study will be critical to developing conservation plans for the existing archeological structures.
Study area
The study area, located on the alluvial plains of the Nile Valley and surrounded by elevated structural plateaus capped by Eocene limestone, is underlain by Paleocene shale (Fig. 3). The alluvial plains generally exhibit flat surfaces that gently slope northward. The average ground surface elevation is about 75.5 m above the mean sea level, but rises to about 79 m at the fringes of the Nile Valley. These alluvial plains can be differentiated into (1) a densely cultivated younger plain occupying the central part of the Nile Valley and covered by Holocene silt and clay, and (2) an older reclaimed plain covered by Pleistocene sand and gravel (El Hosary 1994; Research Institute of Groundwater 1997).
The near-surface Pliocene–Holocene sediments in the central part of the Nile Valley rest uncomformably on a succession of Late Cretaceous–Early Eocene marine sediments (Fig. 4). The Pliocene–Holocene sediments have been subdivided into different lithological units, each of which was deposited by an identified ancestral-modern river system (Ismail 2003), including the Eonile, Paleonile, Protonile (Q1), Prenile (Q2), and Neonile (Q3).
Two main aquifer systems are distinguished within the Pliocene–Pleistocene in the Luxor study area: the shallow Quaternary aquifer and the underlying Pliocene–Pleistocene aquifer. The Quaternary aquifer is composed mainly of graded sand and gravel and locally the thickness ranges from 5 to 95 m and salinity is about 2.6 mg/L. The underlying Pliocene–Pleistocene aquifer, composed of sand and clay, is the secondary aquifer in the study area and has an average salinity value of 700 mg/L (Ismail 2003).
Geophysical data acquisition and processing
Eighteen VESs were acquired using the Syscal R2 instrument (Fig. 1). The Schlumberger electrode configuration was employed, and the maximum current electrode spacing (AB/2) varied from 300 to 400 m. The VESs were spaced at 0.5 to 1-km intervals. The measurements were taken in the east–west direction, perpendicular to the Nile Valley. The measured apparent resistivities from each VES were plotted simultaneously against AB/2 values on log–log paper in the field for quality control of the data.
A suite of 23 TEM soundings were measured using the SEROTEM system close to the locations of the resistivity measurements. A simple coincident loop configuration was employed; in this configuration, the same loop transmits and receives signals. The loop side length was 50 m. During data aquisition, measurements were repeated several times to ensure a high signal-to-noise ratio.
Due to the lack of boreholes at the study site and in order to roughly control the VES interpretation, the present study used the litho-resistivity model of Ismail (2003), based on two boreholes located about 200 m away from the acquired VESs at the east bank of Luxor. In that model, four litho-resistivity units were characterized: (1) an upper unit of dry silty clay with relatively high resistivity (~20 ohm-m), (2) a lower unit with significantly low resistivity (~4 ohm-m) assigned to the moist silty clay, (3) a thick unit (>20 ohm-m) with high resistivity assigned to the main Quaternary aquifer layer, and (4) a low-resistivity layer (<4 ohm-m) assigned to a secondary aquifer layer (Fig. 5a, b).
The resistivity data were first inverted in terms of one-dimensional (1-D) resistivity-depth models using software described by Zohdy (1989) and Meju (1991). The output models were used as initial models for inverting the nearby TEM data using TEMIXXL (1996) software. The resultant TEMIXXL models were used again as initial models for inverting the resistivity data in RESIST (Vander 1988) software. The misfit errors between the measured and calculated models for the whole data set range from 2.8 to 7.3% (Fig. 5c, d). This iterative method was continued until reliable resistivity-depth models were obtained that seemed to be consistent with the subsurface geologic setting. The final models were interpolated to generate 2-D resistivity cross sections, parallel and perpendicular to the Nile River.
VES and TEM results
Based on the joint inversion of resistivity and electromagnetic data, two geoelectrical resistivity cross sections were generated, one parallel to the Nile River and the other perpendicular to the Nile (Figs. 6, 7). The geoelectrical resistivity cross sections exhibit four geoelectrical units. No significant lateral resistivity variation was found within individual units:
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1.
The first (upper) geoelectrical unit consists of (1) a relatively dry silty clay agricultural soil less than 4 m thick with resistivity values ranging from 5 to 28 ohm-m, and (2) dry silty clay and gravel soil, having a resistivity value of 50 ohm-m and a thickness of 2 m.
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2.
The second geoelectrical unit consists of sand, silt, and gravel of the main Quaternary aquifer. The average resistivity value is 20 ohm-m, and thickness is about 48 m. The thickness of the aquifer layer decreases significantly toward the west plateau.
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3.
The third geoelectrical unit is characterized by low-resistivity value (<5 ohm-m) and thickness ranging from about 4 m near the Nile River to about 48 m near the western plateau. This unit represents the secondary aquifer in the study area (Pliocene–Pleistocene aquifer). The significant resistivity contrast between the Quaternary aquifer and the underlying Pliocene–Pleistocene aquifer is attributed to the higher salinity (700 vs. 2.6 mg/L) and clay content of the sediments within the Pliocene–Pleistocene aquifer (Ismail 2003).
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4.
The fourth geoelectrical unit is characterized by a resistivity value of about 10 ohm-m. This unit appears only at the base of the plateau area at a depth of 2–5 m. This unit represents the Paleocene shale layer. Its low resistivity is due to the lateral seepage of groundwater from the adjacent Pliocene–Pleistocene aquifer. A normal fault separates the third and fourth units, and this fault was traced on the resistivity section of Fig. 11. The location and orientation of this fault seem to be consistent with the major fault forming the Nile Valley in this area (El Hosary 1994).
The inverted resistivity, or “true” resistivity, of each of the specified geoelectric units was mapped to better demonstrate the lateral resistivity variation with depth and its possible impact on the degradation of the area’s monuments.
Resistivity distribution at 1 m depth
The first unit represents the dry silty clay topsoil. The resistivity values of this unit vary from 5 to 75 ohm-m (Fig. 8). Although surface conditions, such as farming and urbanization, affect resistivity distribution, the values still provide a good indication of the moisture and/or salinity distribution within the topsoil, which is in direct contact with the archeological features. The high-resistivity values of 25–75 ohm-m are observed near the urban areas (parallel to the Nile River) and near the limestone plateau. The low-resistivity values of less than 24 ohm-m are found for the central cultivated areas in the study site. These low values are a direct result of increased-moisture content due to irrigation and increased salinity caused by excessive evaporation and use of fertilizers.
Resistivity distribution at a depth of 4 m
This unit has resistivity values range from 3 to 29 ohm-m and is characterized by three main resistivity zones (A, B and C), which correspond to the second, third, and fourth geoelectrical units, respectively (Fig. 9). Resistivity values range from 10 to 29 ohm-m for Zone A, which represents the saturated sand and silt sediments of the Quaternary aquifer. The water within this aquifer seems to be fresh and originating from the Nile and irrigation canals (e.g., Asfon canal) in the study area. The resistivity value is low (5 ohm-m) for Zone B, which represents the Pliocene–Pleistocene aquifer in the study area. Zone C, representing the Paleocene shale, has resistivity values ranging from 8 to 16 ohm-m, probably because of its high-moisture content and/or salt.
Resistivity distribution at 48 m depth
This unit has low-resistivity values ranging from 1 to 7.5 ohm-m. Although the range is narrow, Zones B and C are obvious, as shown in Fig. 10. Zone B resistivity values range between 2.5 and 7.5 ohm-m. This zone is probably an extension of the Pliocene–Pleistocene aquifer that consists of sand with clayey sediments. Zone C, which corresponds to the moist Paleocene shale layer, exhibits a very low-resistivity value of 2 ohm-m.
To better visualize the surface and subsurface at the study site, we constructed a composite model that shows the spatial resistivity distribution of subsurface geoelectrical units, the surface location of temples, cultivated areas, and the Nile River. As shown in Fig. 11, the Nile River does not contribute to the groundwater recharge in the study area, since the resistivity values of different strata increase toward the east (i.e., toward the Nile), which is consistent with the conclusion of Ismail (2003). The groundwater flow seems to flow from west to east, and, in the surface layer, from the cultivated areas outward.
Chemical analysis of the water samples
Results of the chemical analysis of water samples can be integrated with the geophysical interpretation to yield valuable information on the causes of increasing salinity and groundwater level at Luxor study area. Six surface water samples were collected from the study area from the Nile River, the canals, and the sacred lake of Memnon Temple. The results of the chemical analyses are presented in Table 1. The sources of different ions in the examined water could be grouped as follow.
Cultivated lands
Sodium (Na+1), an essential constituent used in fertilizers (e.g., Phillips et al. 2001), was 195 ppm in water sampled at Memnon Temple compared with 36 ppm from the River Nile. The high-sodium concentration observed at the temple is evidence that the water inside the monument migrated from the nearby cultivated lands.
Potassium (K+1) is an essential plant nutrient (e.g., Mengel and Kirkby 1980). Potassium is highest (3.5 ppm) in the water sample taken from Memnon Temple, again supporting the interpretation that this water migrated from the surrounding cultivated areas.
Sulfate (SO −24 ) is derived from gypsum, acid rains, and fertilizers (Garg 1978). The highest concentration (96 ppm) of sulfate is observed at Menmon Temple, indicating that its water probably comes from nearby cultivated areas.
Chloride (Cl−1) is mostly presented either as salt crystals or in solution (Na+1 and Cl−1 ions) (Hem 1970). The concentration of chloride ranges from 21 ppm at the eastern side of the study area to 190 ppm at Memnon Temple. The high concentration of chloride at the temple is related to the successive accumulations of water inside the temple that probably migrated from cultivated areas.
Weathering of monuments/temples
Calcium (Ca2+) and magnesium (Mg+2 ) are the principal minerals forming carbonate rocks such as limestone (CaCO3) and dolomite (CaMg [CO3]2). The highest calcium (22 ppm) and magnesium concentrations (18 ppm) were observed at Memnon Temple, probably due to the dissolution of carbonate rocks forming its stone foundations.
Bicarbonates (HCO −13 ) are formed when carbon dioxide is dissolved or derived from limestone (e.g., Rogers et al. 1985). The bicarbonate concentration of water sampled from the Nile River is 122 ppm; from the irrigation channels, 134 ppm and at Memnon Temple, 354 ppm. The high concentration of bicarbonate at Menmon Temple is because of the dissolution of the limestone of its stone foundations.
Natural sources
The pH value of water is a measure of the concentration of hydrogen ions (H+). The pH values of the water samples from the study area vary between 8.2 and 8.3, indicating alkalinity and the dissolution of calcium and magnesium ions in the water samples (e.g., Psenner 1988). Electrical conductivity of surface waters increases from east (320 micro S/cm) to west at Menmon Temple (1,120 micro S/cm). Water with high-electrical conductivity contains sodium and magnesium cations as well as calcium, chloride, and bicarbonate anions (e.g., Freund et al. 1993). As expected, total dissolved solids (TDS) was highest (716.8 mg/L) in the water sample collected from the sacred lake of Memnon Temple and lowest (204.8 mg/L) in the water samples from canals in the eastern side of the study area. The high-TDS value from the Memnon Temple is due to the evaporation of the water in the temple’s sacred lake.
Discussion and conclusions
The joint inversion of VES and TEM data and the results of chemical analyses of water samples were successfully integrated to generate a suite of geoelectric resistivity cross sections and subsurface maps. The main disadvantage of the employed techniques is the limited spatial subsurface coverage and the uncertainty when generating the 2-D cross sections. Obviously, 2-D/3-D techniques (e.g., resistivity and ground-penetrating radar) would produce more subsurface coverage and more accurate models. Those techniques, however, are probably not the best choice at this site given the large survey area, time constraints, and most importantly, because the goal of this present study is not the detailed hydrogeology of the field site. Furthermore, the methods employed in the present study are inexpensive, data acquisition is quick, and achievable penetration depth can be very deep (depending on AB/2 spacing and the loop size of the TEM survey).
Study results indicate that the shallow subsurface in the Luxor study area is divided into four distinct geologic/hydrologic units. Such characterization represents the foundation of any plan to lower the groundwater level and decrease the salinity of capillary soil moisture in the area of the Luxor monuments. Shallow groundwater flow paths were expected to have originated from the recently cultivated areas, west of Luxor and to flow toward the River Nile. The elevated groundwater in the area of the temples appears attributable to flood irrigation of recently reclaimed lands lying on the alluvial/flood plain transition. The progressive increase in salinity along the groundwater flow path is reflected in the recent deposition of precipitated salts observed at Habu Temple (Fig. 2). Based on our interpretation of the acquired data and the field observations, the salt accumulation on the foundations of the monuments appears to be ascribable to salt transport by capillary water from the relatively high-salinity groundwater or from connate water in the silty clay unit.
As a final comment on the study area, recommendations are to avoid cultivation of crops that require much water and to regulate the use of agricultural chemicals in the areas of thin silty clay soil. Further recommendations are to conduct high-resolution geophysical surveys (e.g. 3-D electrical resistivity) and detailed chemical analysis of the water proximal to the Luxor monuments. These suggestions might reduce the groundwater discharge at the temple areas and reduce its effects on the stone foundations.
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The authors thank three anonymous reviewers and the associate editor for their comments that helped improve the quality of this manuscript.
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Elwaseif, M., Ismail, A., Abdalla, M. et al. Geophysical and hydrological investigations at the west bank of Nile River (Luxor, Egypt). Environ Earth Sci 67, 911–921 (2012). https://doi.org/10.1007/s12665-012-1525-2
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DOI: https://doi.org/10.1007/s12665-012-1525-2