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Line source multi tracer test for assessing high groundwater velocity

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24<strong>Line</strong> <strong>source</strong> <strong>multi</strong> <strong>tracer</strong> <strong>test</strong> <strong>for</strong> <strong>assessing</strong> <strong>high</strong> <strong>groundwater</strong> <strong>velocity</strong>68Einat Magal 1, 2 , Noam Weisbrod 1 , Alex Yakirevich 1 , Daniel Kurtzman 3 and Yoseph Yechieli 2101214161 Deptment of Environmental Hydrology & Microbiology, Zuckerberg Institute <strong>for</strong> WaterResearch, Blaustein Institute <strong>for</strong> Desert Studies, Ben Gurion University of the Negev,Sede Boqer 849902 Geological Survey of Israel, 30 Malkhe Israel St., Jerusalem 955013 Institute of Soil, Water and Environmental Sciences, Agricultural Research Organization,Volcani Center, Bet Dagan 502501820Corresponding author: einat.magal@gsi.gov.il22


Abstract24A segmented line-<strong>source</strong> <strong>multi</strong>-<strong>tracer</strong> injection is suggested as an effective method <strong>for</strong><strong>assessing</strong> <strong>groundwater</strong> velocities and flow directions in sub-surfaces characterized by <strong>high</strong>26water fluxes. Modifying the common techniques of injecting a <strong>tracer</strong> into a well becamenecessary after natural and <strong>for</strong>ced gradient <strong>tracer</strong> <strong>test</strong>s ended with no reliable in<strong>for</strong>mation on28the local <strong>groundwater</strong> flow. The <strong>tracer</strong>’s line-<strong>source</strong> increases the likelihood of success of the<strong>test</strong> and could provide additional in<strong>for</strong>mation regarding the lateral heterogeneity of the30aquifer.In a field experiment conducted in the northwestern part on the Dead Sea coast, <strong>tracer</strong>s32were injected into an 8-m long line injection system perpendicular to the assumed flowdirection. The injection system was divided into four separate segments with four different34<strong>tracer</strong>s. An array of five boreholes located within a 10x10 m area downstream was used <strong>for</strong>monitoring the <strong>tracer</strong>s' transport. Two dye <strong>tracer</strong>s (Uranine and Na Naphthionate) were36injected in a long pulse of several hours into two of the injection pipe segments. Two other<strong>tracer</strong>s (Rhenium oxide and Gd-DTPA) were instantaneously injected into the other two38segments. The <strong>tracer</strong>s were detected 0.7 to 2.3 hours after injection in four of the fiveobservation wells, located 2.3 to 10 m apart from the injection system, respectively.40The <strong>groundwater</strong> <strong>velocity</strong> was determined to be ~70-120 m/d, based on the recoveries ofthe <strong>tracer</strong>s. The <strong>groundwater</strong> flow direction was derived based on the arrival of the <strong>tracer</strong>s and42was found to be quite consistent with the apparent direction of the hydraulic gradient.442


Introduction46Understanding <strong>groundwater</strong> flow is essential <strong>for</strong> proper management of <strong>groundwater</strong>re<strong>source</strong>s and monitoring its quality and quantity. Water-level data is often scarce due to the48limited number of boreholes, resulting sometimes in a simplistic and non-reliable view of the<strong>groundwater</strong> flow field. A direct estimate of <strong>groundwater</strong> flow <strong>velocity</strong> and direction is50possible by tracing the migration of a conservative <strong>tracer</strong> that has been injected artificiallyinto the aquifer. The simultaneous injection of more than one <strong>tracer</strong> into the aquifer can be52beneficial since different transport properties of the different <strong>tracer</strong>s can be revealed.Monitoring the <strong>tracer</strong> concentration can be done in the injection well (dilution <strong>test</strong>) and at54observation wells downstream. The <strong>tracer</strong> <strong>test</strong> can be conducted either under the naturalhydraulic gradient or under pumping conditions (<strong>for</strong>ced gradient) in order to increase the56recovery of the <strong>tracer</strong>s. Tracer <strong>test</strong>s were conducted in aquifers ranging from a small scale ofmeters (Halevy et al., 1967; Molz et al., 1988) to hundreds of meters (LeBlanc et al., 1991;58Mackay et al., 1986). Tracers have been injected into aquifers through single or <strong>multi</strong>pleboreholes (3-9 boreholes) at the same location (Dillon et al., 2000; LeBlanc et al., 1991;60Mackay et al., 1986; Maloszewski et al., 2003) as well as through open sinkholes and sinkingstreams (Connair and Murray, 2002; Magal et al., 2008a; Yesertener and Elhatip, 1997).62Depending on the hydraulic properties of the aquifer and the hydraulic gradient, <strong>groundwater</strong>velocities in aquifers vary from less than a centimeter a day (Ronen et al., 1991) to a few64centimeters a day (Mackay et al., 1986; Mallants et al., 2000) and up to a few tens of meters aday (Ptak and Teutsch, 1994; Yang et al., 2001). A successful <strong>tracer</strong> <strong>test</strong> is based on a careful66and appropriate design, which requires a priori hydrogeologic knowledge of the site andpreliminary transport parameter in<strong>for</strong>mation (Divine and McDonnell, 2005). Appropriate68selection of the <strong>tracer</strong>s is also important (Magal et al., 2008b). However, this in<strong>for</strong>mation is3


frequently not available prior to the experiment and may lead to unsuccessful <strong>tracer</strong> <strong>test</strong>s in70which there is low or no recovery of the <strong>tracer</strong>.This paper suggests a modified method of injecting <strong>tracer</strong>s into the <strong>groundwater</strong> through a72line <strong>source</strong> that is separated into segments, enabling the injection of different <strong>tracer</strong>s atdifferent locations. The practical benefit of the proposed method is increasing the likelihood74of recovery of <strong>tracer</strong>s without a major loss of spatial in<strong>for</strong>mation due to the relatively long<strong>source</strong>. The arrival of the <strong>tracer</strong>s injected from different locations at different observation76wells enables reconstruction of the <strong>groundwater</strong>-flow direction and a better understanding oflateral heterogeneity.78Research areaThe study was conducted in the area of the Fashkha (Zuqim) springs nature reserve, which80is located along the northwestern part on the Dead Sea coast (Figure 1a). The springs emergefrom the alluvial aquifer of the Dead Sea Group (Pliocene- Holocene) along a N-S strip of 3-482km on the western coastline of the Dead Sea. The alluvial aquifer, which is build of alterationof coarse and fine sediment, is bounded in the west by the main marginal faults of the Dead84Sea trans<strong>for</strong>m (Figure 1b) facing the carbonate <strong>for</strong>mations of the Judea and Mt. Scopusgroups. The Fashkha springs system, together with two other groups of springs (Qane and86Samar), are the main outlets of the eastern side of the Judea Group aquifer (mountain aquifer).The hydrological system of the alluvial aquifer has been influenced by the water-level drop of88the Dead Sea during the last decades (Yechieli, 2006; Yechieli et al., 1995). Field evidenceshows a gradual process of springs drying out in the north and the appearance of new springs90in the south, in new coastal areas that were until recently covered by the Dead Sea water(Burg et al., 2006). Burg et al. (2006) suggested that a facies change in the sediment92composition from <strong>high</strong> permeability, coarse grain in the west to low-permeable sediment inthe east decreased the <strong>groundwater</strong> hydraulic connection with the receding Dead Sea and4


94resulted in migration of the springs southward, where coarse sediments reach very close to thepresent Dead Sea shore. The specific flow <strong>velocity</strong> and direction of the <strong>groundwater</strong> in96different parts of this hydrogeological system are questionable due to the lack of data. Kafri(2001) estimated the flow <strong>velocity</strong> of the <strong>groundwater</strong> in the Fashkha reserve, based on98radioactive decay of extremely <strong>high</strong> radon content in <strong>groundwater</strong>, to be 33-40 m/day. Thetotal discharge of the springs was estimated to be 60-70 MCM/y (Rophe, 2003) and no major100change in the springs' discharge was monitored over the years. Better understanding of thehydrological system is necessary due to the ongoing drop of the Dead Sea level, which might102risk the future of the springs as well as the natural reserve fauna and flora.104106108Figure 1: Location map and schematic cross section of the geology and hydraulic connection in theresearch area (after Burg et al., 2006).5


Material and methods110TracersTwo fluorescent dye <strong>tracer</strong>s were used in the experiments: Uranine and Sodium112Naphthionate (Table 1). Both <strong>tracer</strong>s were found to be of relatively low sorption affinity(Magal et al., 2008b), low toxicity (Behrens et al., 2001; Kass, 1998) and can be detected114easily with no interruptions to a minimum concentration of a few ppb. The Uranine wasmeasured in the monitoring boreholes by the CYCLOPS-7 ®submersible fluorometer of116Turner Design that was connected to the Campbell Scientific, Inc CR800 data logger, andmeasurements were taken every 10 seconds. The concentrations in ppb were computed using118the calibration line of CYCLOPS-7 ® measurements in a beaker (5 cm above the bottom) filledwith 1L of solution of known Uranine concentration (1000, 500, 100, 50, 10, 5, 1 ppb and 0).120The fluorescence intensity of Uranine is <strong>high</strong>ly influenced by the solution pH (Smart andLaidlaw, 1977). Although there is no reason to believe that the <strong>groundwater</strong> pH changed122during the field experiments, the more precise results from laboratory analysis were used.Two other <strong>tracer</strong>s: Rhenium oxide (Re) and Gd-DTPA (Gd) were found to be relatively124conservative (Byegard et al., 1999) and can be determined in a concentration of 0.1 ppb. Allthe <strong>tracer</strong>s were purchased as dry powders and dissolved in distilled water. The dissolution of126Re 2 O 7 powder in water creates a solution of Re 2 O 4 - ions (Remy, 1956). The density of theinjected <strong>tracer</strong>-solution was kept lower than local <strong>groundwater</strong> density by 0.0005 g/cm 3128130(24°C) in order to prevent downward movement of the <strong>tracer</strong> due to density differences.Table 1: Tracers general in<strong>for</strong>mationTracer Commercial Name FormulaUranine Fluorescent sodium C 20 H 10 Na 2 O 5Na Naphthionate 1-Naththylamine-4-sulfonic acid C 10 H 8 NNaO 3 Ssodium salt hydrate-ReO 4 Rhenium(VII) oxide Re 2 O 7Gd-DTPA Diethylenetriaminepentaaceticacid gadolinium(III) dihydrogensalt hydrateC 14 H 20 GdN 3 O 10 xH 2 O6


Field site and experimental setup132Observation wells: five observation wells were drilled at 5-6" diameters to a depth of 10 m<strong>for</strong> the <strong>tracer</strong> <strong>test</strong> (Figure 2). The per<strong>for</strong>ated PVC pipes (2" diameter) were installed with a134gravel pack between the drilling well and the PVC pipe. The wells were drilled, using casingand without any addition of fluids (drilling mud or water). During the drilling process,136sediment samples were collected and described in the field. The sediments are composed oflayers of gravel and coarse sand alternating to layers composed of <strong>high</strong>er silt and clay138fraction. The variability in sediment composition is seen in Figure 3. In general, thepercentage of coarse sediment layers (containing more than 96% of gravel sediments) is140significantly <strong>high</strong>er than that of the fine sediments (with at least 15% of silt and clays). Themineralogical composition of the fine sediment fraction is mainly calcite, aragonite and quartz142with a minor representation of dolomite, phyllosilicates, K-feldspar and plagioclase. Quitesimilar coarse sediments with altering amounts of fines were found to the depth of 50-60 m in144two boreholes located 300 m from the experimental area (Burg et al., 2006).Groundwater samples, which were collected after pumping, had a density of 0.9999 g/cm 3146(27°C) and contained 3.0-3.6 g/l TDS (EC 5.5-6.8 mS/cm). The water level was 3.5-4 mbelow the subsurface and 6-6.5 m of the well was saturated. Based on the water level148measurements in the boreholes, an approximate value of the hydraulic gradient wasestablished to have a magnitude of 1.7% and direction of 160°N.7


150152154Figure 2: Location map of the line-<strong>source</strong> injection system with four units (Inj 1 to Inj 4) and themonitoring boreholes (circles with numbers of the boreholes and water levels). The directionof the hydraulic gradient is marked by an arrow.156158160Figure 3: Excavated sediments at the <strong>test</strong> site channel of 4 m depth. Note the altering of sedimentcomposition from coarse and <strong>high</strong>ly permeable sediment to fine and less permeable sediment.8


162164<strong>Line</strong> <strong>source</strong>: A line-<strong>source</strong> injection channel was excavated by backhoe to a depth of 0.2 -0.4 m below the water table (~4 m deep, 1.5 m wide and 10 m long). The dimensions of theexcavated channel were chosen because landslides prevented narrower excavation and limited166the penetration of the channel into the saturated zone to less than 0.5 m. Four units of fullyper<strong>for</strong>ated pipes were installed horizontally in the excavated channel just below the water168table (Figure 4). Each horizontal pipe (2.26 m long and 4" in diameter) was connected bythree vertical non per<strong>for</strong>ated PVC pipes (2" in diameter) to the surface (Figure 4). Following170the pipe installation, the channel was refilled with the same local sediments.172174Figure 4: <strong>Line</strong>-<strong>source</strong> injection pipe system. The injection pipes were installed just below the watertable. The <strong>tracer</strong>s were injected through the segments as follows: Re in Inj1, Uranine in Inj2,Naphthionate in Inj3 and Gd in Inj4.Tracer <strong>test</strong> experiments176Point-injection <strong>tracer</strong> <strong>test</strong>: Two point-injection <strong>tracer</strong> <strong>test</strong>s were conducted, first on 5/3/06under conditions of a natural gradient and the second on 4/9/06 under <strong>for</strong>ced gradient178conditions due to pumping. In the second experiment <strong>groundwater</strong> was pumpedcontinuously <strong>for</strong> 80 hours from well FE111 (Figure 2) at a rate of 43 L/min. The <strong>tracer</strong>s9


180were injected two hours after pumping began. It is worth mentioning that during the entirepumping time, the drawdown in the pumping well was less than 3 cm. In both experiments,182two dye <strong>tracer</strong>s (Uranine and Naphthionate) were injected into two boreholes, FE103 andFE110, respectively (Figure 2). Table 2 summarizes the quantities of <strong>tracer</strong>s used in the184field experiments.The injection of the <strong>tracer</strong>s into the wells followed a procedure described by Ward et al.186(1998) <strong>for</strong> achieving initial homogenous <strong>tracer</strong> concentration in the injection well whilekeeping steady <strong>groundwater</strong> flow during the <strong>test</strong>. In short, the procedure includes injection188of the <strong>tracer</strong> through a tube that was lowered into the bottom of the borehole. The volumeof the <strong>tracer</strong> solution was identical to the saturated part of the tube. There<strong>for</strong>e, after lifting190the tube, <strong>tracer</strong> concentration in the ~6 m water column was relatively uni<strong>for</strong>m.Preliminary laboratory investigation of a 3.5 m saturated pipe in similar spreading192conditions of the <strong>tracer</strong> found that the <strong>tracer</strong> concentration at three depths (on a 3.5 msealed tube) was similar, with a coefficient of variance of less than 7.5% between the194depths. The rate of <strong>tracer</strong> concentration dilution in the injection well was continuouslymeasured by an in-hole fluorometer. Groundwater samples of 15 ml volume were taken196using a Masterflex ® E/S TM peristaltic pump connected to 2 mm tubes lowered into thewells to the different depths. During the first five days, water samples were collected198frequently (once in one to four hours) from the observation wells (from depths of 4-4.5, 6-7 and 9-9.5m) and in the following two weeks less frequently (once a day). All200<strong>groundwater</strong> samples were kept in a dark and cold environment from the time they weresampled until they were analyzed.20210


204206208210212Table 2: Summary of the mass and concentration of the <strong>tracer</strong>s used in the field experimentsTracerInjectedthroughInjected<strong>tracer</strong> mass(g)Tracersolutionvolume (l)Injectionduration(h)C 0(ppm)BHPoint injectionUranine FE103 6.49 1.85 impulse 490Naphthionate FE110 10.81 3.09 impulse 848Segment<strong>Line</strong> <strong>source</strong> injectionReO 4 Inj1 11.5 (of Re) 10 impulse 6583Uranine Inj2 720 720 03:29 524Naphthionate Inj3 400 400 04:17 713Gd-DTPA Inj4 15 (of Gd) 15 impulse 215214<strong>Line</strong>-<strong>source</strong> <strong>tracer</strong> <strong>test</strong>: The line <strong>source</strong> experiment (20/7/08) started with the injectionof the four different <strong>tracer</strong>s into the four individual segments of the line <strong>source</strong> (Table 2).216The two fluorescent dye <strong>tracer</strong>s (Uranine and Naphthionate) were injected <strong>for</strong> a few hours(Table 2) by pumping <strong>tracer</strong> solution into three 2 mm diameter tubes that were lowered218into the <strong>groundwater</strong> through the injection system’s vertical pipes (Figure 4). The injectionrate of the solution of the Uranine was 224 ±38 g/hr, whereas the Naphthionate injection220was uneven in time (60-280 g/hr) due to some technical problems. Two other <strong>tracer</strong>s (Gd-DTPA and ReO 4 ) were injected in a short pulse by pouring the solution into the three222vertical pipes of the injection segments. The time of injection and the amounts of <strong>tracer</strong>sused are listed in Table 2. After injecting the <strong>tracer</strong>s, <strong>groundwater</strong> samples were taken224every hour from the line-<strong>source</strong> injection system and from the monitoring wells at twodepths (4-4.5 and 5-6 m). The sampling procedure included collecting 15 ml <strong>groundwater</strong>226samples using the peristaltic pump connected to 2 mm tubes lowered into the wells. All<strong>groundwater</strong> samples were kept in a dark and cold environment from their collection to228their analysis. Sampling was maintained at a <strong>high</strong> frequency of one sample an hour the firstday, a lower frequency of a sample every 1- 4 hours was kept <strong>for</strong> the next 8 days and from230day 9 to day 14 samples were taken once a day. In the FE101 observation well, onlinemeasurement of Uranine concentrations continued <strong>for</strong> another two weeks.11


232Laboratory analysisThe fluorescent dyes were analyzed by fluorescence spectrophotometry (Cary Eclipse234Fluorescence Spectrophotometer, Varian ® , Palo Alto, CA). The concentration of the dyes wasdetermined by using calibration curves prepared by adding known concentrations of dyes to236the natural <strong>groundwater</strong> of the Fashkha springs. Re and Gd concentrations were determinedby ICP-MS, Elan DRCII (Perkin Elmer Sciex, Canada).238Data interpretationPoint dilution <strong>test</strong>240The requirements <strong>for</strong> properly designed point dilution <strong>test</strong>s are: steady <strong>groundwater</strong> flowduring the <strong>test</strong>, homogeneous distribution of the <strong>tracer</strong> through the diluted volume and lack of242vertical current in the borehole including density driven flow (Halevy et al., 1967, Drost et al.,1968, Gaspar, 1987). The injection procedure was planned to meet these requirements. The244average <strong>groundwater</strong> <strong>velocity</strong> (in the borehole, v * ) was calculated based on diluting theconcentration of a non-reactive <strong>tracer</strong> that was introduced instantaneously into a borehole that246is a function of the <strong>groundwater</strong> flux, the vertical cross section area through the center of thesaturated borehole segment (m 2 ) and the volume of this segment (Freeze and Cherry, 1979).248The average <strong>groundwater</strong> <strong>velocity</strong> in the aquifer (v) is then calculated by dividing v * by theporosity of the aquifer and the distortion factor (α), which takes into consideration the250distortion of the <strong>groundwater</strong> flow field due to the existence of the well (Drost et al., 1968).For a borehole equipped with gravel pack, the α value can be up to four (Gaspar, 1987),252though a value of 2 is widely accepted (Pitrak et al., 2007) and was adopted in the currentwork.12


254Groundwater <strong>velocity</strong> assessment from the <strong>tracer</strong> breakthrough curvesGroundwater <strong>velocity</strong> during the <strong>tracer</strong> <strong>test</strong> was assessed in this study by the following256methods:a. According to the <strong>tracer</strong> arrival time: The <strong>tracer</strong> <strong>velocity</strong> was derived by dividing the258travel distance of the <strong>tracer</strong> along the approximated <strong>groundwater</strong> flow lines by thetime of arrival of the center of weight of the <strong>tracer</strong> breakthrough curve (the recovery of260half of the <strong>tracer</strong> mass).b. Using a one-dimension transport model: The solution of the convection-dispersion262equation using the CXTFIT code (Toride et al., 1995) <strong>for</strong> estimating transportparameters was employed <strong>for</strong> modeling the <strong>tracer</strong> breakthrough curves, assuming the264distance vector between the injection line and the observation point is in the directionof flow. The initial concentration of the <strong>tracer</strong>s (C 0 ) injected in short pulses (Re and266Gd) was the concentration measured in the injection pipes immediately after theinjection.268c. Using a three-dimension transport model <strong>for</strong> the <strong>tracer</strong>s that were impulse injected:<strong>tracer</strong> transport in three dimensions was modeled using the solution of Lenda and270Zuber (1970) <strong>for</strong> an instantaneous injection.C( x,y,z,t)M 1=θ 8π32( t − t')22⎡ ( y − y')⎤ ⎡ − ⎤⎢⎥ ⋅ ( z z')⋅ exp −exp⎢−⎥⎣ 4Dt( t − t')⎦ ⎣ 4Dt( t − t')⎦1D Dl2t1322⎡ {( x − x')− v(t − t')}⎤⋅ exp⎢−⎥⎣ 4D( t − t')272l ⎦274(1)276Equation (1) was derived <strong>for</strong> the advection-dispersion equation describing transport of aconservative <strong>tracer</strong> of mass M (gr) that was released at once at point (x', y', z') at time t'278(hr), θ is the aquifer porosity. D l and D t are longitude and transverse dispersioncoefficients (m 2 /h), x, y and z are the coordinates of the observation well (m). The13


280distances x and y are determined assuming the flow direction is known and is 160° fromthe north. To quantify the accuracy of the model predictions, the modified index of282agreement (MIA) was used as a goodness-of-fit estimator (Legates and McCabe, 1999)together with the R 2 and 95% confidence interval <strong>for</strong> the parameters determined by284solving inverse problem.Assessment of <strong>groundwater</strong> flow direction286The possible spectrum of flow directions of <strong>groundwater</strong> can be estimated simply byconnecting the locations in which the <strong>tracer</strong>s were injected to the monitoring wells where they288were recovered. A representative direction of the <strong>groundwater</strong> flow was calculated as thedirection of the vector that resulted from the addition of the <strong>velocity</strong> vectors, which were290calculated according to the arrival time, distance and direction of the line connecting thecenter of the injection interval and the observation well.292Results and discussionTable 3 summarizes the field experiments and their main outcomes. The results and294interpretations are presented below:Point-injection <strong>tracer</strong> <strong>test</strong>s296In the natural gradient <strong>test</strong>, the <strong>tracer</strong>s were not detected in the monitoring wells. Tracerconcentration declines rapidly in the injection wells; loss of 99-99.9% mass during the first298two minutes of the experiment (concentrations of Naphthionate and Uranine decline from 850to 7.4 ppm and from 90 to 0.3 ppm in 2 minutes, respectively, Figure 5). The fast dilution300prevented using the first data points in calculating <strong>groundwater</strong> flow <strong>velocity</strong> since it did notfit a linear plot on the semi-log sheet (Figure 5). The last water samples contained quite low302constant concentrations of the <strong>tracer</strong> and were not used in the calculation. There<strong>for</strong>e, the<strong>groundwater</strong> <strong>velocity</strong> was computed with 4-5 data points only. The average <strong>groundwater</strong> flow14


304<strong>velocity</strong> was estimated to be 22±3 m/d based on the <strong>tracer</strong>'s dilution curves (Table 4).However, this estimate is questionable due to the problems described above, thus other new306field experiments were conducted to gain reliable in<strong>for</strong>mation.In the <strong>for</strong>ced gradient <strong>test</strong> there was no recovery of the <strong>tracer</strong>s in the pumped water or the308observation wells. The low drawdown in the pumping well (3 cm) suggests that due to natural<strong>high</strong> <strong>groundwater</strong> flow rate in the study area, the maximal pumping was insufficient to distort310the natural flow regime.312314316318Table 3: Summary of field experiments and resultsField experiment Date Results Assessed <strong>groundwater</strong><strong>velocity</strong>Natural gradient 5/3/06 No recovery of the <strong>tracer</strong>s -Forced gradient 4/9/06 No recovery of the <strong>tracer</strong>sPoint dilution <strong>test</strong> 5/3/06 22 m/d<strong>Line</strong>-<strong>source</strong> injection 20/7/08 Recovery of the <strong>tracer</strong>s ~100 m/d320322324Table 4: Groundwater <strong>velocity</strong> assessments based on point dilution <strong>test</strong>s under natural gradientconditionsObservation Tracer Depth Slope v * vwell(m)(m/day) (m/day)FE103 Uranine 4.5 9.0 8.6 21.57 7.4 7.1 17.7FE110Naphthionate9.5 8.8 8.4 21.07 9.6 9.2 23.09.5 11.3 10.8 27.1*the flux through the borehole influenced by distortion of the flow field into the borehole, which iscorrected <strong>for</strong> v - estimated <strong>groundwater</strong> <strong>velocity</strong>.32632815


330332a.334336338340342344346348350352354Figure 5: Tracer dilution under anatural gradient at differentdepths in the injection wells: a.Uranine (FE103), b. Naphthionate(FE111). Groundwater <strong>velocity</strong>was calculated according to theregression lines sketched <strong>for</strong> eachcurve.356A numerical exercise was carried out in order to check whether the field conditions in the358study area can lead to a situation whereby no detectable <strong>tracer</strong> concentrations are found in themonitoring wells. The distribution of the <strong>tracer</strong> plume was evaluated using Equation 1, <strong>for</strong>360<strong>groundwater</strong> velocities of 20 and 100 m/d (see below). The longitudinal and transversedispersion coefficients were taken to be 12 and 0.6 m 2 /d (<strong>for</strong> v = 20 m/d), and 60 and 3 m 2 /d362(<strong>for</strong> v = 100 m/d), which are reasonable values <strong>for</strong> this system (as elaborated below). Figure 6demonstrates that, under the assumption of homogenous medium, the point <strong>source</strong> <strong>test</strong> may364result in no recovery of the <strong>tracer</strong>s due to <strong>high</strong> <strong>groundwater</strong> <strong>velocity</strong> and low transversedispersion.36616


368370372374376378380382384386388390392394396400402404406408398Figure 6: Numerical experiment <strong>test</strong>ing the possible dimensions of the expected plume and thechances <strong>for</strong> success of a point-<strong>source</strong> <strong>tracer</strong> <strong>test</strong>. Uranine concentrations calculated with Equation 1,<strong>for</strong> point injection into the FE103 borehole (contour values in ppb). A snapshot of the Uranine plumeis plotted <strong>for</strong>: A. Four hours after injection <strong>for</strong> <strong>groundwater</strong> <strong>velocity</strong> of 20 m/day and dispersioncoefficients of 12 and 0.6 m 2 /d, longitude and transverse, respectively and; B. One hour after injection<strong>for</strong> <strong>groundwater</strong> <strong>velocity</strong> of 100 m/day and dispersion coefficients of 60 and 3 m 2 /d, longitude andtransverse, respectively. Note that under these conditions the concentrations of Uranine in theobservation wells FE110 and FE101 are too low to be detected.In the given conditions of the <strong>high</strong> <strong>groundwater</strong> flow <strong>velocity</strong> and the existing array ofboreholes there are a few possibilities <strong>for</strong> increasing the likelihood of gaining direct410in<strong>for</strong>mation on the <strong>groundwater</strong> flow field: (1) drilling additional observation wells (betweenFE110 and FE101); (2) drilling a wide pumping well <strong>for</strong> greater pumping discharge, one that412might distort the natural flow lines towards the well; (3) to inject the <strong>tracer</strong>s through a line17


ather than a point, in order to enhance the probability <strong>for</strong> <strong>tracer</strong> recovery in the monitoring414wells. This was found to be a better alternative.<strong>Line</strong>-<strong>source</strong> injection <strong>tracer</strong> <strong>test</strong>416The results of the line-<strong>source</strong> injection <strong>tracer</strong> <strong>test</strong> were much more conclusive than theprevious point-<strong>source</strong> injection. After the injection of the <strong>tracer</strong>s, breakthrough curves could418be detected in four out of the five observation wells (Figures 7-10). The early arrival of the<strong>tracer</strong>s at the monitoring wells, after less than one hour in some cases, was even <strong>high</strong>er than420estimated according to the dilution experiments (20 m/d). The <strong>tracer</strong>s Uranine, Gd andNaphthionate arrived at the FE103 borehole (Figure 7) located close to the injection system422(2 m apart). The irregular shape of the Uranine and Naphthionate breakthrough curves is anoutcome of their uneven injection and the proximity of the observation well to the injection424system. The peak concentrations of Gd arrived at the observation well clearly after less thanone hour (Figure 7). The <strong>tracer</strong>s Naphthionate, Uranine and Gd arrived at the FE110426borehole; Gd peak concentrations arrived after 2.3 hours (Figure 8). Gd was the only <strong>tracer</strong>that arrived at the FE111 borehole (Figure 9) after 1.3 hours. The <strong>tracer</strong>s Re, Uranine and428Naphthionate arrived at the FE101 borehole (Figure 10), after 2, 2.2, and 3.4 hours,respectively. No <strong>tracer</strong> recovery was detected in the FE102 borehole.430Groundwater <strong>velocity</strong>The <strong>groundwater</strong> <strong>velocity</strong> computed directly from the time of arrival of the <strong>tracer</strong>s’ center432of mass resulted in an arithmetic average of 73 and 83 m/d <strong>for</strong> a flow direction of 160° and170°, respectively, (Table 5). Groundwater <strong>velocity</strong> was also estimated by the one- dimension434transport model <strong>for</strong> impulse and long pulse injection (Table 6). Three-dimension transportmodels were used only <strong>for</strong> the analysis of the <strong>tracer</strong>s Gd and Re, which were instantaneously436injected (Table 6). The average <strong>groundwater</strong> <strong>velocity</strong>, calculated by the one- and three-18


dimension models, is 82 and 120 m/d, respectively (Tables 7). Thus, this estimate is <strong>high</strong>ly438reliable and is four to six times <strong>high</strong>er than the value obtained by the <strong>tracer</strong> point dilution <strong>test</strong>(Table 4).440442444446448450452454456Figure 7: Breakthroughcurves in observation wellFE103 <strong>for</strong> the line injection<strong>source</strong> (4 m depth).1. Uranine injected at adistance of 2.3 m.2. Naphthionate injected at adistance of 2.9 m.3. Gd injected at a distanceof 4 m.458460462464466468470472474Figure 8: C/C 0 Breakthroughcurves in observation wellFE110 (4.5 m depth):Uranine injected at adistance of 6.8m,Naphthionate injected at adistance of 7.3 m and Gdinjected at a distance of 6.5m.19


476478480482484486488490492Figure 9: The Gd C/C 0breakthrough curve inobservation well FE111,injected at a distance of8.9m.494496498500502504506508510Figure 10: Tracer C/C 0breakthrough curves inobservation well FE101 (5m depth): Uranine injectedat a distance of 9.2 m,Naphthionate injected at adistance of 10 m and Reinjected at a distance of 8m.20


512514516518520522Table 5: Assessment of the <strong>groundwater</strong> <strong>velocity</strong> derived from the line-<strong>source</strong> experiment according tothe arrival time of the <strong>tracer</strong>'s center of mass.Source Observation TracerVelocity along Direction *wellflow-line of (from north)Arrival timeof peakconcentrationArrivaltime ofcenterof massCorrectedtime (<strong>for</strong>injectionduration) 160° 170°hr hr hr m/d m/dInj1 FE101 Re 2.0 3.3 3.3 67 65 154°Inj2 FE101 Uranine 2.2 3.2 1.5 30 27 169°FE103 0.6 4 2.3 147 130 134°FE1102.5 0.8 121 87Inj3 FE101 Naph 3.4 5.5 3.4 46 42 181°FE103 0.7 4.1 2 81 75 178°FE1105.6 3.5 43 37Inj4 FE103 Gd 0.8 1.4 1.4 107 105 199°FE110 2.3 4.4 4.4 48 44 182°FE1111.3 1.4 1.4 138 122 169°Arithmetic average 83 73 171°Resultant <strong>velocity</strong> vector 96 ** 171°* Direction of the line connecting the center of the injection interval and the observation well** Resultant <strong>velocity</strong> vector length divided by 8Table 6: Groundwater <strong>velocity</strong> and the dispersivity estimations calculated from the breakthroughcurves and the analytical modelsObservation Depth Tracer Velocity a l (m) * a t (m) * R 2 MIA **well(m)(m/d)a. One dimension modelFE110 4.5 Gd 25 3 0.97FE111 4.5139 0.2 0.98FE101 5 Re 65 3.4 0.97Uranine 100 1.5 0.99b. Three dimension modelFE101 5 Re 167 ± 0.4 0.6 ± 0.03 0.038 ± 0.002 0.92 0.996.5140 ± 28 0.6 ± 0.8 0.1 ± 0.9 0.65 1FE103 4 Gd 48 ± 2 5.0 ± 0.8 0.09 ± 0.06 0.89 0.975.5 120 ± 6 0.3 ± 0.2 1 ± 1 0.94 0.98FE110 4.5 123 ± 2 0.3 ± 0.03 0.6 ± 0.2 0.92 0.916 112 ± 9 0.4 ± 0.3 0.7 ± 0.8 0.91 0.98FE1114.5 153 ± 11 5 ± 5 0.01 ± 0.06 0.96 0.97692 ± 1 0.2 ± 0.04 0.7 ± 0.2 0.79 0.79± - 95% confidence interval values* a l, a t - longitude and transverse dispersivities- D l =α l v and D t =α t v** MIA- Modified index of agreement21


The direction and lateral heterogeneity of <strong>groundwater</strong> flow524The aerial distribution of the injected <strong>tracer</strong>s and their arrival to the array of boreholesenables evaluation of the general flow direction of the <strong>groundwater</strong> and the identification of526the lateral heterogeneity of the flow field. The <strong>tracer</strong>s' recoveries were found to be consistentin general with the simplified picture of a hydraulic gradient of 160° towards the south528(Figure 11) as detailed below: (1) the <strong>tracer</strong> Re that was injected in the western segment(Inj1) was found only in borehole FE101 located on the western side of the field experiment530(Figure 11); (2) no <strong>tracer</strong> was detected in the FE102 borehole located in the east of theexperiment field, indicating that <strong>groundwater</strong> flow towards the east was limited; (3) the Gd,532that was injected in the eastern segment (Inj4) was the only <strong>tracer</strong> found in the easternborehole FE111 (Figure 11); and (4) the Naphthionate, which was injected from Inj3, was534found in the FE103 and FE110 observation wells located in the center of the <strong>groundwater</strong>flow direction. The recovery of Gd (Inj4) in the FE103 and FE110 observation wells and536Naphthionate (Inj3) in the FE101 observation well (Figure 11) could have resulted fromsome migration of the <strong>tracer</strong>s along the horizontal injection pipes to the west, as was evident538from the occurrence of <strong>tracer</strong>s in different injection segments (Table 7). A similar<strong>groundwater</strong> flow direction (171°N) was derived from the direction of the <strong>velocity</strong> vector540calculated from the arrival times at the observation boreholes (Table 5).542544546Table 7: The concentration of the <strong>tracer</strong>s in all four injection pipes during the injection.SourceRe Uranine Naphthionate GdppmInj-1 (Re) 6583 63 0.5 0.1Inj-2 (Uranine) 0.02 524 4.0 0.001Inj-3 (Naphthionate) 0 58 3500 n. d.Inj-4 (Gd) 0.0 0.01 0.2 215* Gd and Re concentrations were measured 4 and 7 minutes after the injection and Uranine and Naphthionateconcentrations were measured in the middle of the injection time22


548550552Figure 11: Map of arrival of the <strong>tracer</strong>s to the monitoring wells. The dashed lines represent theapparent direction of the hydraulic gradient derived from the water head in the observationwellsThe transport of Uranine suggests a more complicated flow of the <strong>tracer</strong>, as its554breakthrough curve does not readily fit the general picture of the flow lines described above:(1) Uranine was detected in the FE110 observation well located east of the flow line from the556Inj2 segment; and (2) the concentrations of Uranine recovered in the boreholes (Figure 12a)are inconsistent with their distance from their <strong>source</strong>, namely, Uranine concentration was558three orders of magnitude <strong>high</strong>er in the remote borehole (FE101, 9.2 m apart) than in thenearby borehole (FE103, 2.3 m apart). At the same time, the peaks of Gd concentrations were560on the same order of magnitude and consistent with the distance of the observation wells fromthe <strong>source</strong> (Figure 11 and Figure 12b). This may indicate the existence of a preferential flow562path with <strong>high</strong>er hydraulic conductivity that results in faster <strong>groundwater</strong> flow in a somewhatdifferent direction than the general direction implied by the hydraulic gradient.56423


566568570572574576578580582584586588590Figure 12: A comparison of thebreakthrough curves: a. Uranine(FE101, FE103 and FE110observation wells); b. Gd (FE103,FE110 and FE111 observationwells). Note that the vertical scale ofthe breakthrough curves of Uranineis logarithmic while the scale of Gdis linear.592594Dispersivity values596The experimental result analysis can provide estimations <strong>for</strong> the <strong>tracer</strong> dispersioncoefficient, although this was not a main goal of the experiment. The longitudinal dispersivity598was evaluated in the range of 0.2 to 3 m by modeling the <strong>tracer</strong> breakthrough curves with aone-dimension model (Table 6a). The longitude dispersivities derived by three–dimension600model simulations were in a range of 0.2 to 0.6 m with two exceptional <strong>high</strong> values of 5 m(Table 6b). Yet, the fitted model values <strong>for</strong> the transverse dispersivity were non-unique and602had a wide interval of confidence (Table 6b). It is possible that the <strong>high</strong> values of thetransverse dispersivity reflect the migration of the <strong>tracer</strong> east in the line-<strong>source</strong> injection604system that was wrongly simulated by the model as <strong>high</strong> transverse dispersion. A low value of0.03 m <strong>for</strong> transverse dispersivity was suggested by the "numerical exercise" to simulate the24


606experiment results of no detectable <strong>tracer</strong> concentration in the monitoring wells after pointinjection. This is almost direct evidence placing a threshold value <strong>for</strong> the transversal608dispersivity and is there<strong>for</strong>e <strong>high</strong>ly reliable. It should be noted that in these simulations only aratio of 1:20 could be used <strong>for</strong> the longitudinal and transverse dispersivity, which is lower610than the ratio of 1:10, which is most frequently used (Gelhar et al., 1992). The current lowestimates <strong>for</strong> the longitudinal dispersivity (0.2 m) are consistent with the approximate612dispersivity of 0.5 m, calculated using the empirical relation between the dispersivity valueand the experiment scale proposed by Neuman (1990).614Hydraulic conductivityThe aquifer hydraulic conductivity (K s ) was calculated to be about 1200 m/d using Darcy's616law <strong>for</strong> the measured <strong>groundwater</strong> <strong>velocity</strong> (100 m/day), the calculated hydraulic gradientbased on water heads (0.017) and porosity (0.2). The K s in the study area is in the upper618representative values of K s <strong>for</strong> gravel (2600 m/d, Domenico and Schwartz 1990) and issignificantly <strong>high</strong>er than the value of 30-150 m/d determined by a pumping <strong>test</strong> obtained in620somewhat similar alluvial sediment in Wadi Arugot about 30 km from the study area (30-150m/d, Wollman et al., 2003). It should be noted that this K s value is of the specific gravel layer622in the water table region where the <strong>tracer</strong> experiment was conducted.Conclusions624The segmented <strong>multi</strong>-<strong>tracer</strong> line-<strong>source</strong> injection used in this study increases the likelihoodof recovery of <strong>tracer</strong>s in monitoring wells. This method is especially suitable where a626conventional <strong>tracer</strong> <strong>test</strong> of point <strong>source</strong> under natural or <strong>for</strong>ced gradient <strong>test</strong>s ends with noreliable in<strong>for</strong>mation on the local <strong>groundwater</strong> flow. In the current study, it enabled the628estimation of magnitude and direction of a site-representative <strong>groundwater</strong> <strong>velocity</strong>.Furthermore, while traditional <strong>tracer</strong> <strong>test</strong>s using wells may provide in<strong>for</strong>mation about depth-25


630dependent (vertical) heterogeneity, line-<strong>source</strong> <strong>tracer</strong> <strong>test</strong>s may provide additional in<strong>for</strong>mationabout lateral heterogeneity.632The <strong>high</strong> <strong>groundwater</strong> velocities in the research area (~100 m/d) may be explained by thehydrogeological structure of this area, in which large volumes of water are drained from the634mountain aquifer in the west. The drainage to the east is limited due to the impermeable facieschange of sediment composition. There<strong>for</strong>e, the main flow is diverted to the south where636coarse sediment <strong>for</strong>mations reach very close to the present Dead Sea shore and enable betterdrainage of the <strong>groundwater</strong> (Burg et al., 2006). Flow of <strong>groundwater</strong> in a relatively narrow638aquifer strip, between the mountain aquifer and the Dead Sea, may lead to <strong>high</strong> <strong>groundwater</strong><strong>velocity</strong>. The proximity to the shallow fresh-saline water interface of the Dead Sea may also640lead to convergence of the <strong>groundwater</strong> flow lines and an increase of <strong>groundwater</strong> <strong>velocity</strong>(Yechieli et al., 2001). The K s that was derived from the <strong>groundwater</strong> <strong>velocity</strong> is in the range642of 1200 m/d, that is, in the upper range of gravel sediment K s (Domenico and Schwartz 1990).The line-<strong>source</strong> injection can be used easily in small research areas, possibly as feasibility644<strong>test</strong>s be<strong>for</strong>e large-scale <strong>tracer</strong> <strong>test</strong>s. The application of the method is somewhat limited tolocations of relatively shallow <strong>groundwater</strong> tables due to practical considerations of the646injection system installation. Nevertheless, it is also possible to construct up to a 50 m-deepchannel with a special trencher <strong>for</strong> installation of a line <strong>source</strong> (providing a larger budget648exists) and apply the method to a larger field <strong>test</strong>.Acknowledgment650The authors wish to thank H. Hemo, Y. Mizrachi, S. Ashkenazi, R. Gabay, and Y.Neumeier <strong>for</strong> their technical support in the field. The support given by the graduate students652of BGU during the intensive field ef<strong>for</strong>ts is also appreciated. Many thanks go to O. Yoffe <strong>for</strong>the analytical ICP-MS measurements and to U. Malik <strong>for</strong> technical help. I also thank E.654Krueger from IHF, Freiburg University, <strong>for</strong> the friendship and collaboration in the <strong>for</strong>ced26


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