J LIBRARY UNIVE»SITY OF CALIFORNI>» DAVIS A^. APPENDIX E PRELIMINARY CHEMICAL QUALITY STUDY IN THE MANHATTAN BEACH AREA, CALIFORNIA United States Geological Survey- Water Resources Division Quality of VJater Branch UNITED STATES DEPARTMENT OF THE INTERIOR GEOLOGICAL SURVEY Quality of Water Branch PRELIMINARY CHEMICAL- QUALITY STUDY IN THE MANHATTAN BEACH AREA, CALIFORNIA By Robert Brennein Prepared in cooperation with the California Department of Water Resources Sacramento, California Axigust, 1956 CONTENTS Page Introduction 2 Acknowledgments 9 Description of the area 9 Chemical relations in the water 15 Summary 32 References 3^ ILLUSTRATIONS Figure 1 Location of wells in the Manhattan Beach project area, Manhattan Beach, California 4 2 Geologic profile through the "C" line of wells showing the extent of the Silverado water-bearing zone and variation of chloride and total hardness with sampling depth 11 3 Geologic profile through the "G" line of wells showing the extent of the Silverado water-bearing zone and variation of chloride and total hardness with sampling depth 12 ^4- Geologic profile through the "K" line of wells showing the extent of the Silverado water-bearing zone and variation of chloride and total hardness with sampling depth 13 5 Water-level contours for 1903-0^+ and I9U5 in the Manhattan Beach area ih 6 Trilinear plot of selected analyses from the Manhattan Beach area -^-T 7 Calcium, magnesium, and chloride concentrations in the leach of core material from the Silverado water-bearing zone with a sodium chloride solution and sea water 19 TABLES Table 1 Mineral constituents and related physical measurements of the ground water of the Silverado water-bearing zone in the Manhattan Beach area, selected samples of oil field brines and ocean water, CaJ.ifornia 5 2 CsLlculated mixtures of native water with ocean water and oil field brines for selected analyses from the mxmicipal well 8, Manhattan Beach, California 22 3 Calculated mixtures of native water and ocean water for selected analyses from the "C" line of wells, Manhattan Beach, California 26 k Calculated mixtures of native water and ocean water for selected analyses from the "G" line of wells, Meinhattan Beach, California 27 5 Calculated mixtures of native water and ocean water for selected analyses from the "K" line of wells, Manhattan Beach, California 28 -1- PRELIMINARY CHH-IICAL- uALITY STUDY IN THE MANHATTAN BEACH AREA, CALIFORNIA ' 5 By Robert Brennan INTRODUCTION In 19011. Mendenhall (1905) made a survey of the ground water conditions in southern California. At the time of his survey the piezoraetric surface in the area was above sea level, but since that time water levels have declined. During the 1920' s, years of rapid development, the water levels declined at an increasing rate • However, because of decreased pumping during the depression years of the 1930' s, the levels tended to recover somewhat. During the war years of the 19U0's, a large expansion of industry occurred in the area, and ground water withdrawals greatly increased. By 19ii5 water levels in some areas had declined as much as 70 feet below sea levels In the coastal region this heavy with- drawal and the ensuing dry years rapidly lowered the ground water levels, reversing the normal seaward flow of the underground water to a landward flow. In 19hO a definite increase in the salinity of the ground water was noticed at the i-ianhattan Beach municipal well field. The salinity increased over the years until most of the original wells of the field had to be abandoned. In 19U7 Poland, Garrett, and others (1959) made studies of the contamination of the ground water in the Manhattan Beach area and concluded that the contairdnating agent was most likely ocean water. -2- The State of California with its many coastal basins has been most conscious of the value of its ground-water supplies. The possibility of sea-water encroachment into these underground reservoirs has been recog- nized, and means to prevent it have been and still are being sought. In 1950 the California State Legislature appropriated $700,000 for the experimental work connected with the study of this problem. The Manhattan Beach area was selected as the site for experiments to study the feasi- bility of creating a fresh-water barrier close to the coast to prevent sea-water encroachment. The work of this project was carried out by the Los Angeles County Flood Control District under contract with the State Water Reso-orces Board and under the supervision of the California Division of Water Resources. The study involved the injection of Colorado River water from the Metropolitan Water District into a line of wells roughly parallel to the coast and tapping only the main confined aquifer, thereby building up a "pressure ridge". In the course of this workj nine 12-inch injection vrells and thirty-six S-inch observation wells were drilled. Figure 1 is a map of the area showing the location of the wells. As a part of this investigation,, I66 samples of the ground water were obtained from the wells prior to the injection of the fresh water and were analyzed by the Uo S. Geological Survey. In addition, as each well was developed chloride, conductance, and density determinations were made in the field by the Los Angeles County Flood Control District. Many analyses of water from the Manhattan Beach municipal wells also were available. Table 1 presents the analyses of the ground water of the area and selected analyses of ocean water and oil-field brines. 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It is the purpose of this report to review the chemical-quality data obtained in the Manhattan Beach area and to determine whether these data lend support to these conclusions, ACKMOWLEDGMENTS The study described in this report was made by the United States Geolcgical Survey at the request of and in cooperation with the California State Department of Water Resources. It was under the supervision of lo W„ Wallingj District Chemist^ Sacramento^, California, Water samples analyzed by the U.S. Geolcgical Survey were col- lected by personnel of the California State Department of Water Resources and Los Angeles Coijmty Flood Control District, Density;, conductaneej and chloride data made in the field by the Lcs Angeles County Flood Control Distiict and well logs were supplied by the California State Department of Water Resources, DESCRIPTION OF THE AREA The hydrologic data for this section of the report as well as Figure 5 have been abstracted from the report by Poland (1959) on this area. The Manhattan Beach area discussed in this report lies vrithin the West Basin in Los Angeles County, The principal aquifer^ known as the Silverado water-bearing zone, is composed of sandy and gravelly phases of beach and marine deposits of Pleistocene age. Except in the reaches adjacent to the present shoreline, this aquifer is confined under artesian pressure in the Manhattan Beach area,, The confining bed consists of clay on top of the aquifer. The aquifer also is underlain by clay. The Silverado zone is said to be "merged" in this area because the several distinct aquifers present in the zone inland have converged to form a single aquifer in hydrologic continuity m.th the inland aquifers. Figures 2 5 3^ and I4 show the extent of the Silverado zone in the report area. Recharge of fresh water into this aquifer comes mainly from the intake areas inland frdm the Newport-Inglewood uplift^, but some local penetration of rainfall also recharges the aquifer. The Newport-Inglewood fault zone, which forms the eastern edge of the West Basin^ acts as a partial barrier to fresh-water recharge to the aquifer. Loxrering the piezometric surface west of the faults will increase the flow across the faults j and conversely ^ lowering the piezometric surface east of the faults will reduce the recharge to the West Basin. At the time of Mendenhall's work the water level in the ViTest Basin was above sea level and that east of the fault zcne was still higher. The ground water flowed across this fault zone and discharged into the ocean. Figure ^ shows the water level for 1903~Oli from the data of Mendenhall as modified by Poland, Since the time of I-iendenhall's workj withdrawal of the ground water in the West Basin has increased, and the water level has declined as shown by the water level in the area for 19h$ (Figure 5). The recharge of fresh water across the Newport-Inglewood ■10- o o _ o I ^ o> o c — o « .2 C TJ o - .c O aj Q. = CO o x> CT c a> ■- — 2 S E ^ 1 lO ® a> j; a. o *^ ^ » "O O > i- (]> — o O W -c I 3 Figure 3 — Geologic profile through the "G" line of wells showing the extent of the Silverado water-bearing zone and variation of chloride and total hardness with sampling depth I 1 1 1 1 r o o. I ' J) ^ a> 'a. £ E o s » c ■o c i 2 o o c o o o o £ o O -D '«^ o O N O •— ■— w o* o o • s ^ 1 1 Figure 5 -- Depth to water for 1903-04 and 1945 in the Manhattan Beach Area, California fault zone also has decreased, owing to the lowering of the water level inland from the faults. A depression in the piezometric surface has formed in the West Basin east of the Manhattan Beach area. This depression inland from the ocean has reversed the normal seaward gradient in the coastal area and allowed sea water to more inland. CHEMICAL RELATIONS IN THE WATER The earliest chemical-quality data available for the ground water in the Manhattan Beach area are from the Manhattan Beach municipal well field. These analyses show that the water as of 1938 was of the calcium and magnesium bicarbonate type. In this report the analysis of the water from the Manhattan Beach municipal well 8 for October 1938 is considered as water native to the Silverado water-bearing zone prior to the present saline contamination. The concentrations of the ions in this water are used in all calculations involving native water. It is not to be construed that the concentration of a single analysis adequately represents all the water of the aquiferj however, large errors will not be introduced by using a single analysis because, generally, the chemical quality of ground water at a selected sampling point does not undergo marked changes with time unless contaminated, and the total dissolved mineral concentration of the native water is very small compared to the saline"-c.pntaminant in this area. The word contamination is used in this report in the broad sense to cover deterioration in chemical character of the water without regard to concentration or source of the contamination. This broad usage should not be confused with the established usage of the word in the California Water Code (Water Code of 19U9, Division 7, Chapter 2, Definitions). Figure 6 is a trilinear plot of selected analyses of the ground water from the Manhattan Beach area. This plot shows the changes in chemical -15- character of the ground water in the area from 1938 to 1953 and also the change in character of the water coastward from the Manhattan Beach mimicipal well field o Hie principles involved and the procedures used in plotting the chemical character of waters on this type of plot have been described by Piper (I9ii5). Chemical data for the water of the municipal well field in 1938 plots just to the left of center in the central diamond of the figure, and later analyses of water from the same well plot away from the native water approximately in a straight line and toward the top of the diamonds The total dissolved mineral content of the water has increased and the percentage concentration of the ions expressed in equivalents per million has changed « Percentage changes in the cations of analyses 1 through 10 shown in the left- hand triangle have been small. The calcium and magnesium have increased by approximately 10 percent and the percent sodium has decreased by an equal amount. The anion percentages, as shown in the right-hand triangle, have undergone large changes. The bicarbonate-type water originally present has progressively changed to a chloride-type water. The sulfate percentage has remained relatively constant, producirig a straight-line plot in the triangle. Plotting analyses of water from project wells closer to the ocean produces a new plot in the diamond. These analyses plot in a line along the edge of the diamond, descending downward from the apex to a point which represents essentially undiluted sea water. Generally, as the locations of the wells approach the ocean, the analyses of these well waters approach that of sea water. -16- u f o o o M M O o ■> m o o o K «1 o o o o ol O m o o O O O o • o o o o ^5 o • • ♦ • • o M • • O N » • • • M • m t • M « • • • • M O « • e 3 lO A • « • M O • t Q at u • « • -> • M V O « O a. • * • 0» • • • t • m • • 1 • m 1 • 1 • 1 • a • • w O • m m m • 1 1 ■• • m K m • o LE «j M 10 • ** o « • ".St 2 9 "' f • 3 M M N n o « o « • •i • O o m O O - m • o o • * d N w O • m m • • 4 ft M & • cn N m M M o • a • M o O • ♦ e a • • e • • • M m u. • M P* m a • CU e o M 0> 0' • ■ s « • -9 • • M • • • m m m * • m a • ■ a , ■ • • > M 1 M • • • • * - M n ♦ n « K • • o - M ♦ o x: o o a; GO c o o c o 0) E o to <1> «/) _>\ o c o o to cl o c I CO 3 Simple mixing of the native water with sea water or an oil-field brine vrould give a series of plots approximatinp; a strair^ht line .ioininp the native water and the sea water or brine. Obviously, simple mixing of sea vfater or a brine with the native vrater has not taken place. No single type of water vjill produce a (louble-line plot such as this by simple admixture of tv/o vraters. The chemical change may be that of cation exchange. This ty|)e of change requires that ion-exchange materials bo present in the Silverado zoneo Several core samples of the Silverado water-bearing zone were obtained from wells 11-I8 and H-I6 and tested for exchange materials. The sediment samples were obtained from three different depths in each vrell and thoroughly mixed » The dry material was placed in a column and Icachod Tifith distilled water until most of the soluble material was removed, as indicated by a decrease in hardness of the leachate to 100 opiu, a liter of sodium chloride solution of approximately the concentration of sea water was introduced i.nto the coliamxio lihcn the silver nitrate test indicated tho orcsencc of chloride in the leach, samples 1 • i^ve collected and analyzed for calcium, magnesium, and chloride. iJ'igure 7a siovis the results of these analyses. .aximum ion exchange apparently took place in about two hours and then steadily decreased '.irith time. The maxiii:;um exchange noted (between 9 and 11 hours) was slightly less than the concentration of sodium in the solution addedo The core material was regenerated with a calcium ciJ.uri'Jij solution and again rinsed i/ith distilled vjabor unt i rinse showed n total hardness of approximately 100 npiri. .'. litni- - ' I. ;cn introduced at the top of the column and samples of leach collected and -18- lAJUUL Calcium Magnaiiu n i ^ 1^ a I E. -J Bi il ~6 7 i 9 TB — n Sompling timt in hour* Figure a — Calcium, magnesium, and chloride concentrotlons in the leoch from the Silverodo water- bearing zone core motenol leached with a sodium chloride solution ^00 /< Chlorid» / 15.000 200 i \ 1 Calcium Mognttium 10.000 100 1 -l -] \ I _ 5.000 / i X -J 1 1 1 . .. i 1 ' 1 5 6 Sampling ttmt in houri Figure b — Calcium, mognetium, and chloride concentrotiont in the leach from the Silverado water-bearing zone core materiol Itachtd with sto water analyzed as before. The flow through was faster during this second run. Figure 7b shows the results of these analyses. As with the sodii:m chloride solution, ion exchange took place rapidly increasing to a maximum and then decreasing. After about five hours, the leach attained a calcium and raagnesium concentration of the sea xrater added. Because the column was regenerated with a calcium chloride solution, it should not be inferred from the sea-water data that the magnesium of the sea water exchanges for the calcium of the soil. This aspect of ion exchange was not investi- gatedj only the possibility of ion exchange was sought. The postulation that ion exchange is the mechanism by which the observed chemical phenomena can be exolained is supported by these tests showing that minerals capable of entering into ion-exchange reactions are present in the Silverado water-bearing zone. The double-line plot of the trilinear diagram can be explained on the basis of ion exchange coupled with simple mixture. The contaminating water, as it moves through the Silverado zone, undergoes cation exchange. In the resulting mixture of native and contaminating water the percentage of calciiim plus magnesiiim wi-11 remain constant or increase to a maximum if the inflow of contaminating water steadily increases. When this maximum point is reached, the high sodium content of the contaminating water causes the percentage of sodium to increase in the mixture until the contaminating water constitutes 100 per cent of the mixture. Sea water and oil-field brines are two possible sources of contamination in the Manhattan Beach area. Hydrologic evidence favors sea water, and if this is valid, chemical-quality data also should support this conclusion. -20- There are oil wells north, west, and southwest of the Manhattan Beach area. Samples of brines from these fields (Table l) are lower in sulfate and higher in carbonate than sea v/ater and plot below sea water in the trilinear diagram. Selected analyses from the Manhattan Beach municipal well eight were compared with hypothetical mixtures of native water and sea water and native vjater and oil-field brines. These hypothetical mixtures were calculated by determining the percentages of contaminating water and native water required to produce a water whose chloride content in equivalents was equal to the equivalents of chloride of the water actually analyzed. Table 2 compares the analyses with the hypothetical mixtures of native water with sea water and oil-field brines. These data show that the sum of the equivalents of calcium and magnesium in the natural well water exceeds the sum of these ions in the hypothetical mixtures, and this difference increases as the total dissolved mineral concentration increases. Similarly, the equivalents of sodium in the natural well water is less than the equivalents of sodium in the hypothetical mixt\ires in all instances, and this difference is approxi- mately equal to that for the calcium and magnesium. This indicates that ion exchange has taken place as well as simple mixture. The hypothetical mixtures of sea water and native water indicate that the loss of sodium and potassium ions is slightly larger than the gain of the calcium and magnesium ions and that this difference is equal to the loss of the anions bicarbonate and sulfate. This loss can be explained as precipitation of salts from solution. If the sodium ions of sea water exchange for calcium, barium, strontium, etc, of the soil and any of the ions later precipitate from solution as the carbonates or sulfates, the apparent loss would be in sodium carbonate and sulfate. -21- s -6 Pi s n o a «^ d -9 n I 1 «& ^•31 o^. SO V\rH CNJ HUMA :3 COOO O iHvO 3) to s r* O vC -^ n^o-^ \0 f^o^ K J^ W ■Hoc 8- 1 A » ac 0} to n .§9 t. %-• V 1 » a » XA'^Os r- r-l 0-=t r- fHsOlA f^ Os a r^-rriA r^ CM r- J r^ t^rr\yO v.5^ o^ ;> QJ ffi CO COU\| M o^ou^ H H\A33-=f L 03 t> 4^ CO 43 B O t-vO'XA mvOlA v> & t^Heo n~i ^ oo r^ -^-d !* r +' H t! rt H H ■fr t 33 o a ad o O T) ,sg Vh ^^5 2 ^ * ^^ h\ cn O OO o cs> r^oo e OsOsf^; H CJ O evj H H CO |§g & CJ CJOD ^ -sJHCD t3 ■*■ 1 1 fl k 0) -H •H u 4^ £ o (d c ::§ 0\ 1— 1 -3 CJ iH t^ 3o\A r- B r-co H O o 0^ eg s- ^o cO_^ r^Hoo s +> U O « & ^515 O h > k (, n) 0\0 C\J H r^vooo <*% ^£^0O CJ-^vO 1 00 e-cj CO 0\ OO 0\ + (-111 + ■(Hoc a 0) o -o z3 w ^ H H rt ii: H «< o^ gi S n > •H (V 4^ k M nl ■gs « S » I s? k Q> f-i S\ o ta ^ « 9 y T?^ = s 33^ •5 CO r-H H On OJ H + + H r- o CJ ci H .3 g .3 .5 t-d c n) fo r^ 0) bD bO (0 ♦ rH n -H •^ H rH 55 The hypothetical mixtures of native water and brine indicate that the gain of the alkaline -earth ion is larger than the loss of alkali ions and that the difference is almost equal to the gain of sulfate ions. The solution of calcium sulfate from gypsum deposits in the Silverado zone would provide an explanation of this gain. That this has not been the case is evidenced by the net loss of sodium carbonate in the less contami- nated water and not a gain of calcium sulfate, and by the low sulfate concentration in the native water. This would not be expected if gypsum deposits were common in the Silverado zone. For this reason sea water seems the more logical contaminating agent. The project wells, which are nearer the ocean than vjell eight, yield more highly concentrated water than do wells farther away. The selected analyses plotted In I'lj^ure 6 shovj that sea-water character is approached with decreasinp dintnnce from the well to the ocean. Analyses A and B are from waters in wells that tap the Silverado zone in the area between the Manhattan Beach municipal well field and the Rosecrans and Torrance oil fields. These analyses do not show increased contamination and, in fact, are similar to native water in concentration and character. This gives further indication that in the I'^anhattan Beach area sea v/ater is the saline contaminant , The ratio of chloride to bromide also f;ives evidence that the contaiainant is sea water. The ratio of chloride to bromide in sea water is about 290 to 1. Host of the water samples collected in the Manhattan Beach area have a chloride-to-bromide ratio between 270 and 310 to 1, The less concentrated waters shov; larger deviations from the sea-water ratio. This probably is due mainly to the error of the bromide determination. In -23- the waters of lo\'j concentration the relative error is larger than in those of high concentration. A review of the manganese content of the waters introduces some interesting facts. The greatest concentration of manganese is found in waters from wells along the injection line and just inland from this line in the vicinity of the "G" injection well. The manganese content decreases seaward and landward from this line of high concentration. Generally, the manganese content increases with depth within a particular well. This increase in manganese content probably is brought about by ion-exchange phenomena. The sodium ions of the sea water are exchanging for manganese ions in the materials of the Silverado zone. The greatest manganese concentration seems to occur when the magnesium content is equal to or just exceeds the calcium content. Sea-water contamination of fresh-water bodies is not unique to California. Many coastal areas and island provinces have the same problem. In working vjith these problems over the years, hydrologic data have shox-m that the heavier sea water enters an aquifer at the bottom and does not mix completely. Some island countries obtain fresh water which overlies sea water and, if the pumping is not too heavy, contamination can be prevented. As a part of the study of the Manhattan Beach project a model of a confined aquifer was built by the University of California Experimental Station at Richmond to furnish hydrologic data for a body of sea water trapped inland from the injection line as a fresh-water pressure ridge was being built up. In addition to these data, the model studies also showed that the sea water first would enter the basal deposits of the aquifer and then advance inland as a sloping wedge until it completely filled the -2k- confined zone. Project wells situated in the frontal portion of the intruding sea water provided sampling opportunities v/hich aided in the proof of the viedge theory^ Three concepts can be postulated about the behavior of a vredge of saline water moving against a body of fresh vrater in an aquifer; (l) The depth to sea water below a horizontal plane should be less near the coast than inland; (2) any fresh vjater remaining in the aquifer will be found in the uppermost oart of the aquifer j and (3) a zone of mixed sea vjater and fresh v/ater should be encountered at the sea water-fresh water interface. To obtain the best data on the shape and extent of the intruded body of sea water a static situation would be desirable. However, in practice this is impossible to attain, because pumping the wells disturbs the balance between the saline water and the fresh water causing the waters to mix. Pumping also disturbs the rate of movement of the wedge in the vicinity of the well. Samples of water were collected from the many project vrells at different depths as they v;ere developed. These data lend themselves to some proof of the wedge concept. Three lines of observation v/ells were drilled roughly perpendicular to the line of injection wells and extending inland from the coast about half a mile. Figures 2, 3, and 1; shov; the chloride content and total hardness of selected samples from the "C", "G% and "K=' lines of wells as of February, 1953. The vjater from the more inland vfells had lov;er chloride concentration and the concentration increased with depth in any particular v;ell. The relative amounts of hardness increased inland, indicating greater ion exchange at the saline front, ViHiere the aquifer v/as saturated with sea water, the ion-exchange -25- 5 g b m m I 9 §11 r^ *n<0 rH 'n gss J B CO CM c^oa |ss t 3Sg-° s -4 W t-O s nD On^.^ \Amooa3 n 1- SIS^SS a cjiAir, -3 CM mn oi On ~^^ On ii -^■-a S*! !*S s^ 2 SU 2i2Sia o U\c\(r» H 1 ti- CO ^-^0 On H CM cvj r- H -:? tf* mg IT, «■" ^S^K H^ OS ^-NOU\ to B r^r-i r-i 0\ ■35 t^ H H (^ o '1 ~S3 \n \A sl §sl s Uv "^S \f\ GO H ggsa ; H H h' .-g> ^a NOiA-ar^ oj rl C4 On CN* B cu ri » CNr-l 0 9\ Ov Mil 3 PI w P- .H .-I •t * d H o -H if Si c «♦ m fit '^S s! g u « 3 o c X » ^ il s! -H OD N X nO <^ J.5 sl X 00 C\J n ad NO -3 U S^8 OVM CM p ;;33 CO CiJO »* -3 O W*> \Ar-CM H IMI ^a^ sag "^ W '-AH ""3 s ■^nO CM CM M N • - 559'; s;:); fniAH H ^N M in 9n» OsOI P- o w c • » « |3fe £^ m r. m no* ^^ 1^^ ' _ e .1* HI 1 ^^Sg^g « SBiS s t^CM HOO o cvi o\(a d m r-l CNO -3 a -^:2 s sd li •f f f^OD CJ\0 On 00-3^ CO 1 CM f-U« cvj>o (S ^» S ^Ng (S So sl O « -P 1 5SSF1 518:S ■XI X rHOO s^r ^ \0 r^ _ £0O OnOn t- A ! -^S f-OsCvtCM o NO 03 vO O w'^ rS-^lrxO !M CW O^Os cv d 03 Osf^CJ rr\ CMU\_3 (n ii m>Oco Os »n\A o- W r^ m r- §1 111 X r-t <& C\J o f^O (*• 1 CI O i CM_3 CM tn KS (E> CJ »n a sl. P * -ii &8S CCj O r-iOO c^ i r-i_3-^ H CD Q C--0\ H Of^ NO W (no NO « ^C^ !^ S"^ + ? U\ 'J\CV «P;^^K (H H (n-O o M*^ E <^ \j\fx^ f' !.5 e sig^**^ <3 CM (no NO if NO lArH NO ;h J VA lA lA S.S m to ■*» sgg t-vO <7\tA r- lJ-\Orn s e J Oj. M^ o lAOO t^ awsj e sO (-- f^ff) nO rJ>Ovo NO TJ VAVA Hoaco CTv -33 6\ r^ J -3" i» COU\mCN( OtOa r-l H w _ 3^ ^£ t--0OO. O OnO i-t O e. csj r^r-r- JS e< CO (^(4^0 t- cl^i r- Sfr H 0\p- S s So sl V 01 -p &SS ri *«^0\0^ e\j U\r-o Ci s OnO l—f^ CD C^OnUI °2 l«g 8- CO ^-^J^o^ O CJ tHNO o ^ On CM lA \i\q\ u> S »-i CO u\ tA ^"^ _ z * 1 + + fa B S^SS -s. & »M^ eg (nNO lA 4 III! u n -d M ■3 «> V 0) ■P -P "O ■3 ^-^ '^* " 5 ■P (9 (0 -H 4^ 5: nj n rt O -^i^ O tiO 01 bU •3 §,"3 Ch t^ u o u "1 ^ ti^S 3 "m 2 K. 1 J. H rl &> -*- c ! ? •=1: 9l - i - a> 0) -p ■s.^■&^ o ^-rnO o S8g 1 On CM (n*n On cO CM t^ * lA ^f-tCO <*\ |»8 1-4 rH Sc CM p- • • HCD *nU^CM rH o\ OOOCOOO CM CM 1 1 + 1 ^l g £«^a CO o ^^~. S ^5 e ^CM^A (^ f^Hco (n U H H •sia « 9^ 9 o c O t^COCM eo.au\ i^ 1 -3 0-30 o\ O CVJNO Ov _3 CM CO rH u\ -3NOJA \A 1^^ H-3 vO \A NO S CM r- do\ _3 t-mrn HOO Cni H r- \A<*\ t- y> 1 (C r- 0-= o t^C^> On c «4 r4 CTn ^ ~3S S>o in r-\ m -3 ^\A _3\ArH«0 ^w so lA ON CO i-i r^H H •■ (nc^ 1 1 3~ NO NO r-l f nC eo-3u% t^ 1 CM O'NO f^ r4 O On H isis" ^ "SR ^ ■3& -3 r\ -3 3 a sl V « -P |83 1 (O Cti (noc COUMA CUOD-3 S ac CM r- asis^' s i S!^ »€££ ^ m + 1 £■3 1 ^S^8 a CMU\-3 NO CM_3 A t-ONOCN i CM r-o 8 -3 J^« ■^^ liii 'n P -p -9 5 nij -3 o -3 ■S -H ■.^■^■ ■P eg (« '*-( +; >: R] c: <0 o 10 -a w o § ^ fe o MOM rH 0) O (R a o f-t e-» + t. %h X t^ s ^ s°s ■P r-l H Is; s Ik H =: •a capacity of the materials was exceeded and no further evidence of ion exchange was apparent. Tables 3, h, and 5 present the chemical analyses for the water samples from the several wells and the hypothetical mixtures of native water and sea water having the same chloride content. The analyses from the "C" line of wells show that the water from wells C-9, C-5, and C was essentially sea water. The water from well C~k at 77 feet below sea level was approximately 87 per cent sea water with greater hardness than the more seaward wells. The water from 53 feet below sea level vjas approximately 68 per cent sea water and had a slightly higher hard- ness. Further inland at well C-8 the water from Ii7 feet below sea level was less than twice as concentrated as the designated native water, where- as the water from 95 feet below sea level xras about 76 per cent sea water. The water from $2 feet below sea level in well C-12 ^^ras less concen- trated than the dilute water from well C-8 and the water from 92 feet below sea level was only 36 per cent sea vrater compared to 68 per cent for water at that depth in well C-8. The calcium and magnesium percentage increased markedly in the water from well C-12. The analyses of the water from the "G" line of wells show that the aquifer inland to v;ell G-5 was essentially sea water for the total thickness. The water at 71 feet below sea level from well G-3 v:as about 92 per cent sea water but water from 123 feet below sea level was essentially sea water. The water at 76 feet belo^^^ sea level from well G-1 was about 90 per cent sea water and showed increased hardness. A water sample from hS feet below sea level in well G-2 was approximately 38 per cent sea water and relatively high in hardness, whereas the water from 66 feet below sea level was about 86 per cent sea vrater and exhibited a smaller percentage -29- of calcixim and magnesium. Water from 30 feet below sea level in well G-U was approximately three times as concentrated as native water but at 73 feet below sea level the water was 80 per cent sea water. Water at 105 feet belovi sea level in well G-l; was essentially sea water o Water from U8 feet below sea level in well G-8 was approximately the same as water from 30 feet below sea level from well G-I4.. The water at 86 feet below sea leA^el in well G-8 showed increased concentration with continued pumping. After four hours of pumping the water vjas about 12 per cent sea water, but after 20.5 hours it increased to 2? per cento This illustrates the change in the rate of movement of the saline water under conditions of p'omping. The analyses of the water from the "K" line of wells show that the water in wells K-9 and K-5 was essentially sea water. The water from UO feet below sea level in well K-5 was only 8? per cent sea water, indicating that the aquifer was not completely filled with sea water in the total thickness of the aquifer. The analysis of water from well "K" was obtained from 2hS feet below sea level. This is apparently below the base of the Silverado water-bearing zone, and the mixture of water from the Silverado zone and a deeper, relatively uncontaminated aquifer probably accounts for the lower concentration. No water samples were obtained at lesser depths from this well. The water from well K-I4 at $0 feet below sea level was about 67 per cent sea water whereas the water from depth 69 feet below sea level was 89 per cent sea water. The relative hardness was greater in the less concentrated water at shallow depth. At 77 feet below sea level in well K-8 the water vras 68 per cent sea water but at 90 feet below sea -30- level the water was 75 per cent sea water. The relative hardness of these waters was higher than for the waters from well K-U and decreased with depth within the well. The vjater from vfell K-12 at 06 feet below sea level came from the "200-foot sand", and was essentially native water. The upper water-bearing zone in Figure h is the "200-foot sand" which merges with the Silverado zone near the coast to form the single merged Silverado water-bearing zoneo The water from 85 feet below sea level was obtained from the Silverado zone and ivras 28 per cent sea water. The relative hardness of this water was very high. The analyses of water from well K-l6 seem to show rather anomalous results. The water at 78 feet below sea level was about 10 per cent sea water whereas the water from 128 feet belovj sea level was only about tvjice the concentration of native water. The cause of this anomaly is not knovm. The vjater samples collected from the wells in the "G", "G", and "K" lines show to a large extent that chemical-quality data do substantiate the hydrologic conclusions of an advancing wedge of saline water into the confined aquifer. More complete sampling in wells farther inland un- doubtedly vrould provide better evidence of the existence of a saline wedge. ■31- SUMI4ARY Years of decreased rainfall and increased ground-water use have brought about a rapid lowering of ground-water levels in the West Basin of Los Angeles County. The lowering of water levels has reversed the normal seaward gradient of the ground water to a landward gradient in the VJest Basin thereby allowing sea water to encroach into the ground- water reservoir. In 1950 the California State Legislature appropriated $750^000 for the study of means to prevent sea-water encroachment of ground-water basins. The Manhattan Beach area was selected as the site to study the feasibility of creating a pressure ridge of fresh water near the coast to hold back the sea water. The chemical -quality data obtained from the project wells have been reviewed and interpreted. These data support the previous con- clusions made from hydrologic evidence that sea water is the contaminant and that the relatively dense sea water will enter a zone in the shape of an advancing vjedge. Chemical-quality data from the Manhattan Beach municipal well eight indicate that the concentration of dissolved minerals in the water has increased over the years and that the chemical character of this water has approached the character of sea water. Comparison of the contaminated water with hypothetical mixtures of sea water and native water indicate that simple mixing has not taken place but that the sodiijim ions in the sea water have probably been exchanged for the calciiun and magnesium in the sediments. The calcium and magnesium percentages are higher and the sodium percentage is lower than would be expected from simple mixture of native fresh water and sea water. •32- Core samples of material from the Silverado water-bearing zone v;ere obtained and leached with a sodium chloride solution approximately the concentration of sea water and with a sample of sea water. These data show that minerals capable of entering into ion exchange reactions occur in the Silverado zone. Analyses of water from wells close to the ocean and oil fields show that contamination increases in the direction of the ocean and not in the direction of the oil fields, thereby substantiating other observations that the source of contamination is sea water. Chemical-quality data of waters from wells normal to the coast show that the contamination increases with depth in the vrell. In most places essentially native fresh water was found in the upper part of the aquifer. The depth to the saline water body increased with increasing distance inland. This increase in deoth to the saline water body in a landward direction indicates that saline water ;-7as entering the aquifer in the shape of a sloping wedge. The chemical-quality data obtained in the Manhattan Beach area substantiate the previous conclusions of encroaching sea water and lend support to the hypothesis that sea water will enter a confined zone as an advancing wedge. -33- REFERENCES Mendenhall, W. C, 1905, Development of underground waters in the western coastal plain region of southern California: U. S. Geological Survey Water-Supply Paper 193. Piper, A, M., 19^5, A graphical procedure in the Geochemical interpre- tation of water analyses: Trans. Am. Geophysical Union, I9I4.U, pt. 6, p 91U-923. Poland, J. F., Garrett, A. A., and Sinnott, Allen, (1959), Geology, hydrology, and chemical character of the ground waters in the Torrance - Santa Monica Area, Los Angeles County, California: U„ So Geological Survey Water-Supply Paper lit6l. -31^- f^' THIS BOOK IS DUE ON THE LAST DATE STAMPED BELOW RENEWED BOOKS ARE SUBJECT TO IMMEDIATE RECALL MAR 1 6 19^'^' 8197f All^ Z^^ MAR 2 7 ISW'O JUN 1 8 1982 RECEIVED iECEIVLD JAN i i^^^ PEcr:ivE:x) fHYSSClLIBRMRV DEC 1 t^O ecyi^»y"'« LIBRARY, UNIVERSITY QF CAUFpWfPR^VlS Book 'slip-2dm-8,'«4CT623B4)458 Fr.V2 3Ct UBPJARV 3 1175 00661 4930 '.^\\^rY\\^, PHYSICAL SCIENCES LIBRARY C! Z LIBRARY UNIVERSITY OF CALIFORNU Davis 240490 fl .:^