JournalofHydrology:RegionalStudies9(2017)163–182
ContentslistsavailableatScienceDirect
Journal
of
Hydrology:
Regional
Studies
jou rn a l h om ep a ge :w w w . e l s e v i e r . c o m / l o c a t e / e j r h
Temporal
changes
in
groundwater
quality
of
the
Saloum
coastal
aquifer
Ndeye
Maguette
Dieng
a,c,∗,
Philippe
Orban
a,
Joel
Otten
a,
Christine
Stumpp
b,
Serigne
Faye
c,
Alain
Dassargues
aaHydrogeology&EnvironmentalGeology–DptArGEnCo,Aquapole,UniversityofLiège,4000Liège,Belgium
bInstituteofGroundwaterEcology,HelmholtzZentrumMünchen,IngolstädterLandstrasse1,D-85764Neuherberg,Germany
cDepartmentofGeology–FST,UniversityofCheikhAntaDiop,Dakar,Senegal
a
r
t
i
c
l
e
i
n
f
o
Articlehistory:
Received27April2016
Receivedinrevisedform7December2016
Accepted10December2016
Keywords:
Groundwatersalinization
Selforganizingmaps
Geochemicalprocesses
Environmentalisotopes
Salouminverseestuary
a
b
s
t
r
a
c
t
Studyregion:GroundwaterinthesouthernpartoftheSaloumBasininSenegal.
Studyfocus:TheSaloumestuaryisahypersalineand‘inverse’estuarywherethesalinityof riverwaterincreasesintheupstreamdirection.Thisregionisproblematicinthatdueto theunderlainsuperficialContinentalTerminalaquiferborderedbythehypersaline estu-aryconstitutestheuniquefreshgroundwaterreservoirforwatersupplyforitsestimated 466,000residentslivingin18ruraldistricts(belongingtotheregionsofFatick,Kaolack andKaffrine).ThisisofhighvaluegiventhatthedeepMaastrichtianaquifer(200–300m depth)issaline.Thisstudyaimstodescribeandunderstandtemporalchangesinthe chem-icalandisotopiccompositionsofgroundwater,thegeochemicalprocessesandespecially thegroundwatersalinization.
Newhydrologicalinsightsfortheregion:Theanalyticaldatawerediscriminatedinto3groups onthebasisofthewatertypes.Na-Cl,Ca-ClandCa-SO4richwatersderivedfromsaline waterintrusionatthevicinityoftheSaloumRiveraccompaniedbyionexchangereactions andpollutiondominatethefirstgroup.Thesecondgrouplocatedmainlyinthecentre andeasternpartsoftheregionisfeaturedfreshgroundwaterofCa-HCO3derivedfrom calcitedissolutionreactions.ThethirdgroupofNa-HCO3typeandlessmineralizedindicates fresheningprocessesbyrecentlyinfiltratingrainwaters.Slightseasonalchemicalvariations areobservedduetonewinfiltratingwaterreachingthewatertable.
Highvariationinrainfallbetweenthe2referenceyears(2003and2012)alsochanges chemicalpatternsinthegroundwater.Chemicalevolutionofthegroundwateris geographi-callyobservedandisduetoacombinationofdilutionbyrecharge,anthropiccontamination andseawaterintrusion.Theresultsofenvironmentalisotopes(␦18O,␦2H)comparedwith thelocalmeteoriclineindicatethatthegroundwaterhasbeenaffectedbyevaporation pro-cessesbeforeandduringinfiltration.Theresultsalsoclearlyindicatemixingwithsaltwater andanevolutiontowardsrelativefresheningbetween2003and2012insomewellsnear theSaloumRiver.
©2016TheAuthors.PublishedbyElsevierB.V.ThisisanopenaccessarticleundertheCC BY-NC-NDlicense(http://creativecommons.org/licenses/by-nc-nd/4.0/).
∗ Correspondingauthorat:DepartmentofGeology–FST,UniversityofCheikhAntaDiop,Dakar,SenegalandHydrogeology&EnvironmentalGeology
–DptArGEnCo,Aquapole,UniversityofLiège,4000,Liège,Belgium..
E-mailaddresses:nmdieng@doct.ulg.ac.be,ndeye81.dieng@ucad.edu.sn,diengmaguette@yahoo.fr,mdmaguettedieng@gmail.com(N.M.Dieng).
http://dx.doi.org/10.1016/j.ejrh.2016.12.082
2214-5818/©2016TheAuthors.PublishedbyElsevierB.V.ThisisanopenaccessarticleundertheCCBY-NC-NDlicense(http://creativecommons.org/
164 N.M.Diengetal./JournalofHydrology:RegionalStudies9(2017)163–182
Introduction
TheContinentalTerminal(CT)aquiferisauniquefreshwaterreservoir,whichsupportsvariouswaterneedsintheSaloum regionlocatedmid-WestofSenegal.Unfortunately,thisresourceisthreatenedbysaltwaterintrusionderivedfromboththe oceaninthewesternpartandfromthehypersalineSaloumRiverwhichlimitsthesysteminthenorthernpart.TheSaloum hydrologicsystemisatide-influencedinverseestuaryinwhichhighevaporationratescombinedwithlowflowinthis contextofflattopographyresultinsaltdepositionandhighsalinityofthesurfacewaterbody.AsdefinedbyPritchard (1967),ininverseorhypersalineestuarysystems,thesalinityoftheriverwatersubstantiallyexceedsseawatersalinity. Thispatternisgovernedbythenetlossoffreshwaterusuallyresultingfromanexcessofevaporationoverrunoffand precipitation.Thesesystems,forwhichsalinityincreasesupstreamfromtherivermouthtowardsinlandregions,occur mostlyinaridorsemi-aridpartsoftheworld(Largieretal.,1997),suchasAustralia(Wolanski,1986)andWestAfrica (Barusseauetal.,1985;Diop,1986;PageandCiteau,1990;SavenijeandPagès,1992;RiddandStieglitz2002;Mikhailovand Isupova,2008).Therefore,groundwatersalinizationintheseareasiscloselylinkedtodirectsaltwaterintrusionandhigh evaporation.PreviousstudiesinAustraliaevidencedgroundwatercontaminationprocessesthroughestuarinesaltwater intrusionintheSwan-CanningEstuary(SmithandTurner,2001)andinthePioneerValley,NorthernQueensland(Werner andLockington,2004).IntheSaloumregion,Noël(1975)thenDiluca(1976)investigatedthegeometry,flowregime,and chemicalcharacteristicsofgroundwaterintheCTaquifer.Salinitypatternandassociatedgeochemicalprocessesusingbasic ionchemistryweredescribedbyFayeetal.(2001,2003,2004,2009,2010).Theresultspointedoutthatthegroundwater resourceisconstrainedbytheoccurrenceofmoderatetohighsalinityinthenorthern(neartheSaloumRiver)andwestern (coastalarea)partsoftheaquifer.There,manyshallowwellshavebeenimpactedbytheoccurrenceofsalinewater.Further investigationsweredonebyFayeetal.(2004)usingminorelements(B,Br,Sr)andisotopicindicatorstogetherwithsome majorionsforconstrainingsource,andrelativeageandsorption/desorptionreactionsrelatedtorefresheningandsalinization processes.Inthislatterstudy,boronconcentrations(7–650g/L)weretestedagainstthebinarymixingmodel.Results showedsalinizationprocessesareevidencedbyBsorptionandNadepletionwhentheSaloumRiverwaterintrudesthe aquifer(salinization)inthenorthernpartoftheregion.Conversely,BdesorptionandNaenrichmentoccurasthefresh groundwaterflushingdisplacesthesalinegroundwatersinthecoastalstrip(refreshening).Inthecentralzonewhereancient intrusionprevailed,theprocessoffresheningofthesalinegroundwaterwasindicatedbythechangesinmajorionchemistry aswellasBdesorptionandNaenrichment.TherelativelystableisotopeandtritiumcontentsoftheCTaquiferindicatedthat groundwaterisderivedfromrecentprecipitationandmixingwithrecentlyinfiltratingwatersandevaporationcontribute tothechangesinisotopicsignature.
Therefore,salinisationconstitutesamajorissueintheSaloumregionduetothefactthatpotabledrinkingwaterneeds relysolelyontheCTgroundwaterresourcegiventhatthedeepMaastrichtianaquifer(200–300m)exhibitshighchloride contents(500–1000mg/L)andsomehazardouselements,suchasfluorideandboron,whichreachconcentrationsof2–4 and1–2mg/L,respectively(Travi,1988).Therefore,theCTaquiferrepresentsauniqueaccessiblefreshwaterresourceinthe region.
Despiteofthesevaluableresults,temporal(bothseasonalandlongterm)effectswerenotadressed.Therefore,thepresent studyaimsatreassessingthegroundwaterqualitychangesoftheCTaquiferinthelightofthenewconstraints(e.g.changes inclimaticconditionsandpumpingconstraints),andthenewgroundwaterflowpatternconfiguration.Specifically,this studyintendsto:(1)identifyseasonalvariationsinthechemicalpatternsinrelationtogeochemicalreactionsanddilution usingstatisticaltools,suchasSelfOrganizingMaps(SOMs),and(2)assessthetemporaltrendofgroundwaterchemistry andsalinizationusingchemicalandisotopicgroundwatercompositions.
2. Studyarea
2.1. Locationandgeomorphology
ThestudyareaislocatedinthewesternpartofSenegalandcoversthesouthernpartoftheSaloumhydrologicBasin exceptforthemangrovesystem.Thesurfaceareaisapproximately3380km2 (Fig.1)andislimitedtotheNorthbythe SaloumRiver,totheWestbythemangroveareaandtotheSouthandEastbytheGambiaRivercatchment.
Thegeomorphologicsettingwhichconsistsofagentlyslopingplainthatextendstowardthecoastisincisedbyanetwork ofdepressionswhere temporarystreamsdrainrun-offwaterduringtherainyseason.Adigitalelevationmodel(±4m precision)thatwascreatedfromtopographicalmaps(1:50,000)andmeasuredpointsshowselevationsrangingfrom−1m intheWestandtheNorth(nearthemangrovesandtheSaloumRiver)to+50mintheSouthandEasttowardstheplateau zoneborderedbytheGambianBasin(Fig.1).InthenorthernandwesternregionsalongtheSaloumRiverandthecoast, respectively,asuccessionofhighareas(10–30m)anddepressions(0–10m)formsthelandscape.
Landuse/landcoverofthestudyareawereinvestigatedusingOctober2010Landsatimage(ETM)andlineardiscriminant classifier(LDC)supervisedclassificationmethod(Diengetal.,2014).Surfacefeaturesgeneratedcompriserainfedagricultural crops(52%),naturalvegetation(40%)(composedofsavannah,woodedpark,bushlandandshrubsteppetrees),dispersed habitationspredominantlyvillages(3.5%),saltybarrensoilslocallycalled“tanne”(2%),surfacewaterbodies(1.5%)and mangroveecosystemareas(1%).
N.M.Diengetal./JournalofHydrology:RegionalStudies9(2017)163–182 165
Fig.1. Locationoftheinvestigatedareaandmonitoringnetwork.Thedarklineindicatesthelocationofthecross-sectionA-A’presentedinFig.2.
2.2. Climate
Theclimateoftheregionistropicalwithtwodistinctseasons:adryseasonfromNovembertoMayandarainyseason fromJunetoOctober.Theaverageannualrainfallfrom1960to2012variedfrom750mminthesouthernpartofthebasinat Niorostationto615mminthenorthernpartatKaolackstationwithaSouth-Northdecreasinggradient.Therainfallrecord (Fig.3)atKaolackstationcomparedtothemeanreference1960–1990showsahumidperiodfrom1928to1971followed byadryerperiodfrom1971totheendofthe1990s,whichoccurredthroughmostoftheSahelzone.InsomeSub-Saharan countries,suchasthestudyarea,thisdryperiodwasfollowedbyprogressivelywetteryears(LebelandAli,2009).
Availableclimaticdata(i.e.,precipitation,temperature,relativehumidity,insulation,andwindspeed)fortheperiodfrom 1981to2012collectedfromtheSenegalNationalMeteorologicalAgencyattheKaolackandNioroweatherstationsshow thattheaverageannualtemperaturerangesfrom28to29◦C.Theaverageannualpotentialandactualevapotranspiration valuescalculatedusingthePenmanmethod(Allenetal.,1998)are2030and552mm/yrrespectively.
2.3. Hydrology
ThehydrologicsystemoftheregionismainlycomposedbytheSaloumRiveranditstwotributaries,theBandialaand DiombossrRivers.TheNemaRiver,whichistheonlyperennialfreshwaterstream,flowstowardstheBandialaRiver(Fig.1). Itreceivesagroundwaterbaseflowofbetween0.012and0.03m3/sduringthedryandrainyseasons,respectively(Ngom, 2000).Downstreamtheseriversandstreams,smallseawatercreekslocallycalled“bolons”occurinadditiontothelarge low-lyingestuarybearingtidalwetlands,andthemangroveecosystem.Asdiscussedpreviously,theSaloumestuaryisaninverse estuary.MeasurementsdataduringthedryseasonshowedthatthesalinityoftheSaloumRiverincreasesfrom36.7g/Lat themouthtomorethan90g/latKaolack(located120kmfromthemouth)(Diop,1986).PageandCiteau(1990)usingdata recordrevealedthatsalinityoftheSaloumRiverishighlysensitivetoclimatevariationswithagradientofapproximately 1.3g/lperyearbetween1950and1986(Fig.3).ThisobservationisinaccordancewithworksofSavenijeandPagès(1992) inwesternAfricaninverseestuarieswhichevidencedsharpincreaseinsalinitygradientsduringtheSaheldroughtsinthe 1960s.
2.4. Geologicalandhydrogeologicalcontext
ThestudyareabelongstotheSenegalese-Mauritaniansedimentarybasin,whichisthelargestcoastalbasininnorthwest AfricaandbearsformationsfromtheCretaceoustotheQuaternary(Bellion,1987).Thegeologicalcontextoftheregion
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Fig.2.CrosssectionofthestudyareashowingthegeologicalformationandthepiezometriclevelofCTgroundwater(crosssectionindicatedinFig.1).
hasbeenstudiedusinglithologicalinformationfromboreholesandhand-dugwellsinadditiontoregionalpreviousstudies (Lappartient,1985;LePriolandDieng,1985)andarecentregionalgeologicalmap(1:500000)(Rogeretal.,2009).TheCT formations,whicharethefocusofthisstudy,arepresentthroughouttheregionandarecoveredbyathinandyounger Quaternarysandlayerandlocallybyalluvialdepositsintheriverplains.Theseformationsoverlietheimperviousmarl/clay Eoceneformations.
TheCTsedimentsaredetritalmarineCenozoic(Oligo-MiocenetoPliocene)originandshowevidenceofintenseferralitic alterationduringthelateMiocene,includingferruginousconcretions(Lappartient,1985;ConradandLappartient,1987). Theyarelaterallyandverticallyheterogeneousandcontaindiscontinuousinterbeddedsandstone,sandyclay,clayeysand,silt andclay(Noël,1975;Lappartient,1985;ConradandLappartient,1987)(Fig.2).Locally,claysandstonebedsandferruginous crustsarepresentatthetopoftheformations.Kaoliniteformsthecementinthenon-ferruginoussandstoneandsand sedimentsandrepresentsthedominantclaymineral.Goethiteispredominantandformsthecementofthequartzgrainsin theferruginoussandstonehorizon.Tracequantitiesofillitehavebeenidentifiedwhileintheeasternpartoftheregion,the quartzgrainsarecoatedbycalcite(Lappartient,1985).
Hydrogeologically,theCTformationsareconsideredasunconfinedaquiferwhichthicknessincreasesfromNNW(less than50m)toSSE(approximately100m)andfromWest(lessthan50m)toEast(approximately100m)(Fig.2).Theaquifer reservoirliesonanirregularandimperviousEocenesubstratecomposedofmarlandlimestonecoveredbyclay(Fig.2)(Lyand Aglanda,1991;Sarr,1995).Thehydraulicconductivityandstoragecoefficientvaluesobtainedfrompumpingtestdataunder depthaveragedconditionsrangefrom0.5to8.6×10−4m/sandfrom0.5to21×10−2,respectively(Diluca,1976). Thirty-oneboreholeswithpumpingratesbetween10and45m3/handnumeroustraditionalwellsareusedforthewatersupply inthisregionandtotalwithdrawalisestimatedat8000m3/day.Groundwaterrechargeoccursmainlythroughrainwater infiltration.Computedvaluesusingchloridemassbalance(CMB)method(chlorideprofilesatdifferentsitesobtainedduring thecourseofthisstudyandnotshownhere)intheunsaturatedzone,andhydrologicalbudget(ETocomputedbyPenman formula)arevariableandrangefrom17to100mm/yearandfrom19to130mm/year,respectively.Theserechargevalues aresimilartothoseobtainedbyEdmundsandGaye(1994)(11–108mm/year)usingthesameCMBmethod.Thespatial variabilityislikelytobeduetolocalvariationsinsoiltypeandtexture(notablyclaycontents)andtovegetationcover.The CMBapproachuncertaintiesinourcontextcanbelinkedtopotentialClcontributionfromothersourcessuchassaltwater intrusionoranthropogenicinput.Watertablemeasurementswereobtainedduringthe2012campaignsinMay(endofdry season)andinNovember(endofrainyseason).TheywereconvertedtoheadvaluesthroughanaccurateDGPStopographic surveyofthesamplingsites.ItallowstoreassessgroundwaterflowpatternsshowninFig.4forthedryseason.Asimilarflow patternisobtainedfortherainyseason(notshownhere).Head(h)distributionfeaturesthreegroundwatermoundslocated inthenorthwest(9.8≤h≤11.7m),inthesouthwestalongtheupstreampartoftheNemaRiver(25.3≤h≤26.6m),andin theNorth(13.2≤h≤16m).AmarkeddepressionisobservedNorthandparalleltotheSaloumRiver,wherethemeasured
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Fig.3. InterannualvariationoftheSaloumRiversalinity(inred)andofthemeanannualrainfallmeasuredatKaolacklocalityfrom1927to2012modified
fromPageandCiteau(1990).
Fig.4.GroundwaterpiezometricmapintheCTaquiferduringthedryseasonof2012.
headsarebelowmeansealevel(aslowas−4m).Thislatterdepressionisacommonfeatureinmanyunconfinedaquifers insub-SaharanAfrica,suchasinTrarza/Mauritania,inYaere/NorthCameroon,inGondo,Nara,andAzaouad/Mali,andin Kadzell/Niger(Archambault,1960;Degallier,1962;Aranyossyetal.,1989;Ndiayeetal.,1993;Favreauetal.,2002;Ngounou Ngatchaetal.,2007;Koussoube,2010).IsotopicstudiesperformedinMali(Aranyossyetal.,1989),Niger(Favreauetal., 2002)andSenegal(Ndiayeetal.,1993)suggestthatthecombinedeffectsofhighevapotranspirationandlowhorizontal permeabilityarethemaincausesofthistypeofpiezometricdepressionssincepumpingratesintheseareaarelow.
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Fig.5.Rechargemapandpunctualobservedseasonalchangesinpiezometricheads.
Basedonthisconfiguration,severalgroundwaterflowpatternscanbedepicted:
−fromthenorthwestandnorthernmoundstowardstheseaandtheSaloumRiver,wheretheheadvaluesdecreasenear theshorebutarestillpositive;
−fromthesouthwestmoundinalldirections;occurrenceofthegroundwatermoundinthezonesustainstheNema Riverflowduringlowstageperiod(Ngom,2000);
−fromtheSaloumRiverandthesouthernmoundtothepiezometricdepression.
Theseasonalandlongtermheadvariationsobtainedfrom2012(dryandrainyseason)and1973datasetsmayreflect seasonalrechargeandinterannualevolution,respectively.Seasonalheadvariationsrecordedin2012rangefrom0.1to2.8m withthehighestvaluelocatedfarfromthepumpingareainazoneofrelativehighrecharge(>50mm).Thelowestvalueof headvariationisobservednearthepumpingareainazoneofrelativelowrecharge(<30m)(Fig.5).
Comparisonofthe2012headvalueswithheadsmeasuredduringpre-developmentanddriestperiodof1973infew referencepointsshowwatertablerisefrom0.7to6.8m(mean4.2m)(Fig.6).Thisisobserveddespitethepumpingfrom morethan100boreholesandnumerousdugwellssincetheearly70s.Thislongtermwatertableriseprobablyreflects sensitivityofthesystemtoclimateandespeciallytoannualrainfall(440and847mmrespectivelyin1973and2012).
3. Materialsandmethods
3.1. Fieldcampaignsandlaboratoryprotocols
Tocompletetheexistingdataset(includingthedataacquiredin2003),twofieldcampaignswereconductedinMay2012 (endofthedryseason)andNovember2012(endoftherainyseason).Themeasuredandsamplednetworkcomprises forty-fourgroundwatersamplingpoints(composedof5boreholes,35hand-dugwellsand4piezometers)inadditiontothree surfacewatersamplingsitesalongtheSaloumRiver(atFoundiougne(FL1),Lindiane(FL2)andKaolack(FL3))(Fig.1).Prior tosampling,depthtowatertableandphysicochemicalparameterssuchaspH,electricalconductivity(EC)andtemperature (T)weremeasuredinthefieldateachsiteusingamulti-parameterprobe.Thegroundwatersampleswerecollectedafter purgingthepiezometerswhilewellsandboreholesusedforwatersupplydidnotneedtobepurgedbecausetheywere pumpedcontinuously.
Forchemicalanalyses,asetoftwosampleswascollectedforeachpointandsubsequentlyfilteredthrough0.45m membranesintopolyethylenebottles.OneacidifiedtoapHlessthan2usinghighpurityHNO3forcationanalysis,andthe otheronenotacidifiedforanionanalysis.
Forstableisotopeanalysesofoxygen(18O)andhydrogen(2H),selectedpointsofthenetworkandthethreeSaloumRiver pointsweresampledduringthewetseasonandtightlysealedin1-lpolyethylenebottleswithoutfiltered.
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Fig.6. DifferencesbetweenpiezometriclevelsmeasuredinNovember1973andNovember2012in16wells.
Recordsofmeasuredquantityofrainand2012rainwatersampleswerecollectedfrom7climaticstations,namelyKaolack (K),Nioro(N),WakhNgouna(W),Foundiougne(F),Djilor(D),Sokone(S)andToubacouta(T).
Thechemicalanalysesformajorions(Ca2+,Na+,Mg2+,K+,Cl−,HCO3−,SO42−andNO3−)wereperformedusing stan-dardmethodsofflameatomicabsorption,potentiometric,andtitrationattheLiegeUniversityHydrogeologyLaboratory (Belgium).TheEnvironmentalisotopeanalyseswereperformedattheHelmholtzZentrumMünchen,Instituteof Ground-waterEcology(Neuherberg/Germany)usingdual-inletmassspectrometry(Coplen,1988)andresultsareexpressedinthe conventional␦-permil(␦‰)notationwithreferencetotheViennaStandardMeanOceanicWater(VSMOW)withprecisions of±0.1‰for␦18Oand±1‰for␦2H.
3.2. Dataanalysisandmultivariatestatisticalanalysis
Whiletheelectricalconductivity(EC)isroutinelyusedtomeasurethemineralisationofwater,conventionalmethods involvingmajorand minorionsanalysis,ionicratios,and isotopicmethodsareusedinassessinggroundwaterquality (Ghesquièreetal.,2015;Nicolinietal.,2016)andtheinteractionbetweenfreshwaterandsalinewater(Magaritzetal., 1981;Mercado,1985;Kimetal.,2003).
Multivariateanalysismethods,suchasFactorAnalysis(FA),PrincipalComponentAnalysis(PCA)andHierarchical Clas-sificationAnalysis(HCA),arealsooftenusedtoidentifymajorgroundwatergroupsandfactorsthataffectthegroundwater chemistryinaquifers(Mudry,1991;Güleretal.,2002;Belkhirietal.,2012;GambleandBabbar-Sebens,2012;Montcoudiol etal.,2015;Ghesquièreetal.,2015;Ibrahimaetal.,2015).However,thesemultivariateanalysesaregenerallybasedon linearprinciples(Mudry,1991;GambleandBabbar-Sebens,2012)andcannotovercomedifficultiesarisingfrombiases duetocomplexityandnon-linearityindatasetsandfromtheinherentcorrelationsbetweenvariables.TheSOMsmethod (Kohonen,1982)appliedhereisanalternativetotheselattermethodstoefficientlydealwithdatasetsthatareruledby complex,non-linearrelationshipsintheanalysisanddiagnosisofdynamicsystems(HongandRosen,2001;Hongetal., 2004;GarciaandShigidi,2006;Peetersetal.,2007;GambleandBabbar-Sebens,2012;Gning,2015).Itallowsclustering asetofhydrochemicaldataintotwoormoreindependentgroups(Kohonen,1995;).Thismethodoutperformstheother statisticaltoolsinthatitcansuccessfully:1)dealwiththenonlinearitiesofthesystem;2)bedevelopedfromdatawithout requiringmechanisticknowledgeofthesystem;3)handlenoisyorirregulardataandbeeasilyandquicklyupdated;and4) interpretandvisualizeinformationfrommultiplevariablesorparameters(Kohonen,2001).
ThecomponentplanesandU-matrixarevisualizationmapsthatuseahexagonaltopologytorepresentthemainoutput results.Thecomponentplanesshowhighandlowvaluesonastandardizedmaptoidentifycorrelationsbetweendifferent parameters.Ultimately,intheSOMsanalysis,allthesecomponentmapsarecombinedtocreateaunifiedmatrix(U-matrix) thatcharacterizestheEuclideandistancesbetweeneachnode(Peetersetal.,2007;GambleandBabbar-Sebens,2012).The
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clusteringisbasedonavisualinspectionoftheU-matrixwhereclusterscorrespondtodifferenttypesofgroundwater withrespecttothecontributionofeachelement.TheinformationobtainedfromSOMsapplicationcanthenbeusedto highlightwatermineralizationprocessesthatoccurintheaquiferbasedonthedegreeofsalinityandthespatiotemporal hydrogeochemicalvariability.
Inthisstudy,11chemicalvariables(EC,pCO2,pH,Ca2+,Mg2+,Na+,K+,Cl−,HCO3−,SO42−andNO3−)areprocessedusingthe SOMsToolboxoftheMATLABTMcodetofirstinvestigatethevariablesthataffectthesalinityandtheirrelationships.Classical tools,suchasPiperdiagramsandbivariateanalysis,arethenusedtoconfirmtherelationshipsbetweenthevariables.
4. Resultsanddiscussion
4.1. Hydrochemicalcharacteristics
Theresultsfromthein-situphysico-chemicalsurveysand thechemicaland isotopesanalysesofgroundwater, sur-facewater,andseawatersamplesarepresentedinTable1,andthemeanconcentrationsfromtherainwateranalysesare presentedinTable2.Allsampleshaveionicelectricalbalanceslessthan5%,whichconfirmreliableanalyses.
ThesurfacewatersamplesthatwerecollectedatthethreesitesalongtheSaloumRiverhaveaveragepHvaluesfrom7.8 (dryseason)to8.3(wetseason),whichindicateslightlyalkalinecharacteristics.Theaveragesurfacewatertemperatures areclosetotheambienttemperatureandrangebetween28and30◦C.TheECvaluesvaryalongtheriverfrom64,700(dry season)to50,800S/cm(wetseason)atFoundiougne(10kmfromthemouth),from91,700(dryseason)to60,400S/cm (wetseason)atLindiane(90kmfromthemouth)andfrom89,000(dryseason)to55,200S/cmatKaolack(120kmfromthe mouth).TheseresultsshowthatthesalinityoftheSaloumRiversubstantiallyexceedsseawatersalinityvaluesandsupport theinverseestuarycharacteroftheSaloumRiverwithgraduallyupstreamincrease ofsalinity.However,thedecrease observedatKaolackisprobablyduetotheinflowoffreshgroundwaterasshowninthepiezometricmap(Fig.4).
Temperaturesofthegroundwatersamplesrangefrom27.7to30.9◦Candfrom26.4to33◦Cinthedryandwetseasons, respectively.ThepHvaluesvarybetween3.7and7duringthedryseasonandbetween4.6and8.8duringthewetseason. Thelowestacidicvalues(pH3–5)arefoundinwellS49,whichislocatednearthemangrovearea,andcouldbedueto theoxidationofpyrite,whichischaracteristicofmangrovedegradationgroundwaterconditions(Fordetal.,1992).The measuredECvaluesrangefrom74to3430S/cmandfrom47to2040S/cminthedryandwetseasons,respectively. AccordingtoWorldHealthOrganisationWHO(2008),thisbroadrangeofECvaluesdifferentiatestwotypesofgroundwater inthesystem:
1-freshwaterwithECvalueslowerthan900S/cm.Thisgroupcompriseswatersampledfromwellsinthewesternand centralpartsoftheregion;
-salineand/orpollutedwaterswithECvalueshigherthan900S/cm.Thesesamplesoriginatefromthecoastalareas, neartheSaloumRiverandfromafewwellsinthecentralpartofthestudyarea.
4.2. Groundwaterqualityassessment
Theevaluationofthechemicalcharacteristicsofthegroundwatersamplesusingthedescriptivestatisticapproachshows anorderofrelativeabundance(inmeq/L)ofCa2+>Na+>Mg2+>K+andofHCO
3−>Cl−>NO3−>SO42−.Itisthecaseforboth campaigns(dryandrainyseason).Ahighvariabilitybetweentheminimumandmaximumvalues(Fig.7)isobserved.The concentrationsofSO42−andNO3−,andtoalesserextentCa2+,Mg2+andHCO3−,arehigherforthegroundwatersampled duringtherainyseason.Thiswasprobablytheresultoftheinfiltrationofpollutedwaterandthedissolutionofcalciteand dolomiteduringinfiltration.TheconcentrationsofNa+andCl−inthesegroundwatersamplesdecreaseless,whichisprobably duetodilutionbyrechargewater.MostofthemajorionconcentrationsarewithintheWHOrangesfordrinkingwaterexcept forsomecasesinwhichthehighestvaluesofsodiumNa+,Cl−,NO3−andSO42−exceedthedrinkingwaterthreshold.This suggestssalinewaterintrusionandanthropogeniccontaminationasshownbytheECvalues.Theshallowestwells(S23,S49 andS52)arecharacterizedbyhighNO3-contents(195,200and327mg/L,respectively)duetolocalcontaminationfrom domesticwasteandpastoralactivitiesaroundthewells.ThehighestSO42−concentrationof582mg/LisrecordedinwellS49 andisassociatedwithhighconcentrationsofCl−(215mg/L),Na+(111mg/L),Ca2+(214mg/L),Mg2+(53mg/L),K+(46mg/L) andNO3−(200mg/L).ThiswellislocatedatNemavillageclosetothemangroveecosystemprobablyreflectstheimpactof salinewaterintrusionandassociatedprocesses(gypsumdissolutionand/orpyriteoxydation)andanthropogenicpollution atwellhead.
4.3. GroundwaterclassificationusingtheSOMsmethod
TheSOMsmethodappliedtobothdatasets(rainyanddryseasons)exhibitssimilarpatternandinthispaperweonly describeresultsobtainedfromthedryseasoninFig.8aandb.ThecomponentmapsofCl−,Na+,Ca2+andMg2+(Fig.8a)show similardistributionpatternstoECmap,whichindicatesthattheseionsarehighlycorrelatedwithECandthatdilutionisthe mainfactorinducingvariability.ThehighcorrelationbetweenNa+andCl−suggestsacommonoriginfromthedissolution ofhaliteand/orsaltwaterintrusion.Toalesserdegree,HCO3−correlatestoCa2+.ThepHandHCO3−alsohavesimilarmaps but,asiscommonlyfoundingroundwater,areinverselycorrelatedwiththeCO2pressure.
N.M. Dieng et al. / Journal of Hydrology: Regional Studies 9 (2017) 163–182 171 Table1
Physico-chemicalmeasurementsandresultsforgroundwatersamplesandSaloumRiversamples(FL1,FL2andFL3),fordryandrainy(wet)seasonscampaigns,andgroundwaterisotopicdataforthewetseason.
Parameters EC T pH Ca2+ Mg2+ Na+ K+ HCO
3− Cl− SO42− NO3− ␦18O ␦2H
Units (S/cm) ◦C mg/l ‰
ID Dry Wet Dry Wet Dry Wet Dry Wet Dry Wet Dry Wet Dry Wet Dry Wet Dry Wet Dry Wet Dry Wet Wet
S1 688 551 30.3 29.9 5 7.4 22.4 30 8.5 8.8 58.9 55.6 3.6 3.4 9.8 19.5 120.1 106.1 0.9 1.9 59.2 67.3 −4.5 −32.5 S2 612 360 30 29 5.6 6.8 43.9 37 4.9 4.4 38.9 19.3 5.8 2.9 65.9 25.6 76.4 58.5 8.3 1.8 65.5 51.4 S3 493 453 29.5 30.2 6.7 7.4 58.3 70 2.6 3.4 11.5 10.6 1.9 3.2 177.6 188.8 25 26.7 2.6 3.4 1.7 18.5 S4 369 289 29 30.8 6.2 7 39.1 41 2.9 2.9 15 15.7 0.7 0.5 131.4 126.8 23.5 22.8 1.4 1.3 5.9 5.2 S5 388 317 29.4 30.8 6.6 7.6 44 50.3 1.7 1.6 12.9 13.9 2.6 2 149.8 155.6 15.9 17 3.7 3.7 2.2 4.8 S6 185 225 29 29.2 6 7.9 17.8 30.3 1 1.7 12.9 13.7 1.1 2 58.5 106 8.6 9.4 1.1 1.8 9.8 6.7 S17 191 231 28 29.8 5.5 7.2 16.5 27 1.1 1.6 13.7 16.7 0.5 1 36.6 59.7 11.1 14.3 0.2 0.6 28.2 43.9 −5.1 −35.2 S18 570 500 30 31.1 6.6 7.5 81.3 86.3 5 5.3 14.2 14.3 1.8 1.9 300.2 298 9.4 11.9 0 0.6 0 3.4 −5.2 −35.9 S19 341 313 30 30.6 6.5 7.6 50.6 59.4 0.9 0.8 5.3 5.9 4.1 3.7 163 183.2 5.7 7.6 1.3 1.4 0.8 2.2 S20 900 748 29 30.1 7 8.1 116.4 109 9.1 9.3 32.9 30.7 1.1 1 332.9 314.9 79.8 72.2 3.5 3.8 0 3.8 −5.1 −34.7 S21 268 194 29.1 29.7 6.5 7.4 34.3 30.7 1.4 1.8 8.1 7.7 0.9 0.9 101 81.2 8.6 8.1 1.4 0.9 14.1 22.3 S22 980 781 29 29.6 5.5 5.9 51.2 52.1 6.2 7.4 81.1 83.8 1.4 1.3 65.9 64.7 185.4 180.4 10.6 11.4 5 7 −5.1 −35 S23 1040 890 29 29.2 6.2 7.5 109.1 106 11.1 12.1 39.6 40.4 7.9 8.4 162 130.4 86.7 94 3.5 3 176 196 S24 669 575 29.5 29.2 6.5 7.7 72.4 75.2 7.1 6.7 32.7 33.3 1.4 2 227.5 219 58.9 64.5 3.8 5.4 9.4 9.3 S25 296 231 29 33 5.4 7.4 12.6 13.3 1.9 1.8 26.1 25.8 0.5 0.4 17.1 22 25.9 23.6 0.5 0.7 57.5 57.8 S26 391 333 29.2 30.4 6 7.5 39.6 44.8 8.1 8.9 9.8 10.5 3.5 3.8 152.4 156 15.5 19.3 2.1 2.2 9.7 13.5 −5.1 −34.9 S27 294 224 29 31 5.9 7.9 19.3 18.8 2.8 2.8 20.7 20.1 0.5 0.5 46.3 46.3 30.9 31.5 0.9 0.7 22.9 23.2 S28 1160 908 29.2 30.1 7 7.4 113.3 102 17.2 15.2 41.9 39.3 9.3 11.3 194 169.3 191 178.1 0 2.7 0 4.5 S29 490 492 29.8 30.1 6.4 7.3 59.2 71.7 6.1 6.1 13.7 18.8 1.9 5 181.4 222.2 23.5 34.5 2.3 1.8 18.8 10.1 S30 138 98 29.2 31.1 5.5 8 8.4 8.3 3.2 3.4 6.3 6.3 0.5 0.6 26.9 29.3 7.1 8 9.6 10.8 1 1.1 −5.2 −35.5 S32 125 101 29 28.9 5.3 7.8 5.1 5.1 1.1 1.1 14.1 13.3 0.8 1.1 15.9 14.7 6.6 6.3 0.9 0.9 25.3 28 −5.2 −36.7
Parameters EC T pH Ca2+ Mg2+ Na+ K+ HCO
3− Cl− SO42− NO3− ␦18O ␦2H
Units (S/cm) ◦C mg/l ‰
ID Dry Wet Dry Wet Dry Wet Dry Wet Dry Wet Dry Wet Dry Wet Dry Wet Dry Wet Dry Wet Dry Wet Wet
S33 362 308 30.2 30.3 6 7.6 39 43.5 4 4.3 14 14.9 0.8 0.6 104.8 104.8 23.8 26 1.1 1.5 24.6 29
172 N.M. Dieng et al. / Journal of Hydrology: Regional Studies 9 (2017) 163–182 Table1(Continued)
Parameters EC T pH Ca2+ Mg2+ Na+ K+ HCO
3− Cl− SO42− NO3− ␦18O ␦2H S35 827 995 28 28.7 5.8 8.4 28.4 38.5 7.5 11.2 97.3 130.1 4.1 6.6 24.4 22 184 250.3 10 10.9 24.5 32.2 −4.1 −31.2 S36 480 550 29 29 5.8 6.9 31.3 41.5 3.8 5.7 39 55.6 0.7 1.6 39 89 47.2 78.3 4.9 13.2 78.7 54.5 −4.1 −31.7 S37 419 197 29.2 30.6 4.1 8.8 19 25.3 6.1 2.6 27.7 10.6 2.4 2.4 1.9 42.6 62.1 23.9 0 1.2 66.3 24 −4.2 −31.3 S38 730 760 29 30.1 6.1 8 58 74.8 4.7 6 58.4 62.8 0.9 1 87.7 126.7 116.3 139.9 1.6 3.1 39.2 40.1 S39 253 217 30 29.4 5.7 8.6 15 17.9 1.9 2 20.8 22.6 0.5 0.4 48.8 50 23.9 23.3 0.6 0.9 25.2 30.8 S40 184 175 30.5 33.5 4.9 8.4 6.9 10 1.9 2.4 11.9 14.5 6.1 7.4 7.4 11 26 29.1 0.5 1 24.1 28.3 S41 280 286 29.4 29 4.7 8 9.3 18.1 1.5 2.7 23.7 29.4 0.3 0.4 3.9 12.3 31.6 36.5 0.3 1 49.5 68.4 −5 −33.9 S42 528 1583 27.7 26.4 5.2 8.1 28 124.4 6.3 22.5 33.8 138.5 5.6 6.5 13.5 60.9 108.2 390.2 2.3 8.8 12.7 90.3 −4.5 −31.1 S43 216 278 28.7 30 5.4 8.6 11.6 20.2 1.2 2.4 17.3 29.5 0.3 0.3 22 22 23.6 46.3 0.3 1 27.8 48.7 S44 355 332 29.8 29.4 4.9 7.4 14.7 18.5 3 3.9 28.3 34.5 0.9 1.1 14.8 13.5 32 39.1 0 0.6 71.9 86.2 S45 185 147 29.3 29.3 5.7 7.9 12.4 11.4 0.7 0.7 16 15.3 0.5 0.6 36.6 36.6 13.6 13.4 0.7 0.6 17.3 18 S46 342 286 30.1 29.8 4.4 7.2 6.1 7 2.8 3.3 35 37.5 1.4 1.4 5.2 3.8 30.2 34 0 0.6 72.8 80.8 S47 74 58 30.9 31.1 5.2 7.6 1.5 6 0.2 0.3 6.2 4.4 0.6 0.5 12.3 14.7 2.9 3.6 0.6 0.6 7.9 15.1 −5.1 −33.7 S48 3430 239 27.7 28.8 6.7 7.9 260.4 30.9 38.3 0.4 324.3 13.8 3.7 0.1 323.4 34.1 870 47.4 34 3.5 0 0.5 S49 2191 2040 28.9 27.9 3.7 4.6 124.8 213.7 37.5 52.9 91.9 110.6 58.8 45.8 16.3 7.6 173.5 214.9 426.8 583 203.8 200 −4.7 −32.1 S50 111 125 29.6 29.8 5.4 7.5 6.7 14.6 0.5 0.6 7.9 9 0.2 0.1 20.8 48.8 11.5 11.5 0.9 1.1 0.9 0.2 −5.4 −34.9 S51 81 47 30 28.3 5.3 7.8 3.2 2.1 0.2 0.4 6.8 7.3 0.2 0.2 13.5 9.8 2.6 2.8 0.2 0.1 12.1 12.3 −5.2 −34.2 S52 1140 995 28.2 28.7 3.8 5.9 49.2 53.8 14.1 16.6 98.1 90 2.3 4 13.6 6.5 110.1 104.9 1.2 1.6 296.7 328 S53 176 98 29.5 29.3 5.1 7.8 7.2 9.8 1.1 0.9 9.2 8 0.9 0.7 22 24.4 9.2 7.2 1 0.9 12.1 15.7 Parameters EC T pH Ca2+ Mg2+ Na+ K+ HCO3 Cl− SO42− NO3− ␦18O ␦2H Units (S/cm) ◦C mg/l ‰
ID Dry Wet Dry Wet Dry Wet Dry Wet Dry Wet Dry Wet Dry Wet Dry Wet Dry Wet Dry Wet Dry Wet Wet
S62 407 388 29.6 29.6 5.2 6.1 23.3 31.9 5.5 6.8 25.2 26.5 3.6 3.6 25.6 40.2 32.8 34 0.8 1 86 93.3 S64 75 54 29.1 31.3 4.8 6.2 5.8 5.7 0.8 0.8 4 3.9 0.2 0.2 28.2 27 3.6 3.5 0.1 0.1 0.4 0.4 −5.4 −36 Min 75 47 27.7 26.4 3.7 4.6 1.5 2.1 0.2 0.3 4 3.9 0.2 0.1 1.9 3.8 2.6 2.8 0 0.1 0 0.2 −5.4 −36.7 Max 3430 2040 30.9 33 7 8.8 260.4 213.7 38.3 52.9 324.3 138.5 58.8 45.8 332.9 314.9 870 390.2 426.8 583 296.7 328 −4.1 −31.1 Avg 554.18 465.8 29.3 29.8 5.63 7.49 41.49 45.73 5.7795 6.339 36.28 33.6 3.609 3.998 81.03 80.29 70.19 63.11 12.54 16.3 40.35 49.8 −4.1 −31.1 FL1 64700 50800 27 28.9 7.8 8.1 690.7 424.7 2010.7 1226 17455 10389 718.6 383.7 174.8 142.8 29641 16918 4155 2435 0 0 −0.1 −5.4 FL2 91700 60400 30 31.3 7.8 8.3 956 570.1 3679.3 1510 30053 12707 1086 399.8 206.4 151.1 52933 20857 7458 2984 0 0 0.3 −5.3 FL3 89000 55200 28 29.5 7.7 8.4 1162 574.2 4036.6 1241 32652 11443 1195 481.9 215.8 147.1 60183 18518 8540 2840 0 0 0.3 −3.2
N.M.Diengetal./JournalofHydrology:RegionalStudies9(2017)163–182 173 Table2
Physico-chemicalmeasurementsandresultsforseawatersample(sw)andmeanvaluesofconcentrationsfromrainwater((K,N,F,D,S,TandW)analyses.
Parameters CE pH Ca2+ Mg2+ Na+ K+ HCO 3− Cl− SO42− NO3− Units (S/cm) (/) mg/l SW 39250 7.7 338.3 952 7998.9 356.2 149.1 13014 1911.7 0 K 105 6.6 3.5 0.4 2.7 1 19 6.7 2.3 5.1 N 44 6.7 2.7 0.4 0.7 0.2 14 2.3 2.8 3.1 F 17 5.2 0.7 0.1 0.7 0.3 2.2 1.7 2.3 0.8 D 27.2 5.3 1.1 0.2 0.6 1.1 2.9 1.6 4.9 1.2 S 39.8 5 2.3 0.3 0.8 5 3.7 1.5 5.9 2.7 T 24.6 6.2 2.6 0.1 0.4 0.3 8.2 1.3 2.2 1.2 W 34.4 6.7 0.7 0.2 0.5 1.8 19 1 0.7 0.9
Fig.7.BoxplotofmajorionscompositioninCTgroundwaterandcomparisonbetweendryandwetseasonsof2012.
ThreedistinctgroupswereobtainedwiththeSOMsmethod,whichcorrespondtodifferentgroundwatertypeswith
respecttothecontributionofeachchemicalparameter(Fig.8b).Thephysico-chemicalandchemicalcharacteristicsofthese
3groupswereevaluatedusingadescriptivestatisticapproachinwhichtheminimum,maximum,andaveragemedianof theECandmajorionswerecomputedforeachcampaign(Table2).Inadditiontothestatisticalapproach,aPipertrilinear diagram(Piper,1944)thatdescribesthewatertypes(Fig.9),bivariatediagrams(Fig.11aandb)andcomputedSaturation Index(SI)values(Fig.11c)wereusedtofurtherinferthevariousprocessesthatcontrolthechemicalcompositionsofthe groundwatergroups.
TheU-matrix(Fig.8b),Piperdiagram(Fig.9)andTable3showthat:
a)Group1,whichisrepresentedbysamplesS1,S2,S22,S23,S34,S35,S36,S37,S38,S42,S49,S52andS62,ischaracterized byhighvaluesofEC,Cl−,Na+,NO
3−andSO4−andrelativelylowvaluesofHCO3−.ItisgenerallyencounteredneartheSaloum RiverandinonesampleneartheNemaRiver(Fig.10).TheECvaluesrangefrom491to2191duringthedryseasonwith anaverageof872S/cm.Thewatertypes(Fig.9)aredominantlyNa–Cl(42%)andCa–Cl(42%),andtwosamples(S23and S49)exhibitingCa–HCO3(8%)andCa/Na–SO4(8%)facies,respectively.Thisgroupincludessalinewater(S22,S28,S35and S42)thatischaracterizedbyhighCl−contents(oftenabove150mg/L)aswellaspollutedwater(S23,S34,S49andS52)with highNO3−contents(above100mg/L).Itindicatescontaminationofthegroundwaterandrecentinfiltration(Currelletal., 2010).Salinegroundwater,seawaterandtheSaloumRiverhavetypicalcommoncharacteristicsofNa-Cltypewater(Fig.9) andmolarratiosclosetoseawatervalue(0.86)(Fig.11a).Thisfactconfirmsthemarineoriginoftheions(Jonesetal.,1999; Vengoshetal.,1999;Fayeetal.,2001,2003,2004;Vengosh,2013).However,somesamplesexhibitingarelativedeficiencyin Na+relativetoClprobablyreflectreverseionexchangereaction.InthiscaseNa+istakenupbytheclayexchangerandCa2+is releasedtothesolution.MagaritzandLuzier(1985)statedthatgroundwatersamplescontaininglessthan15%seawaterare
174 N.M.Diengetal./JournalofHydrology:RegionalStudies9(2017)163–182
Fig.8.a)SOMsindividualcomponentsmapsofthechemicalparametersintheCTaquiferduringthe2012dryseasonandb)SOMsU-matrixandclustering
in3groups.
enrichedinNa+,andasthepercentageofseawaterincreases.Infact,thewaterbecomesincreasinglyenrichedinCa2+and Na+isdepleted.ThisprocessleadstogroundwaterfaciesevolvingfromNa-CltoCa-Cl(Mercado,1985;AppeloandPostma, 2005).Inaddition,thesampledpointsarealignedalongaslopeof−1inthe(Ca+Mg)–(SO4–HCO3)versus(Na+K)-(Cl-NO3) diagram(Fig.11b).Thisdiagramexcludeshalite,calciteanddolomitedissolution(JankowskiandAcworth,1997;Garcia etal.,2001;Abidetal.,2011)andevidencedionexchangereactionasadominantgeochemicalprocess..
ThecorrelationbetweenCa2+andSO42−(Fig.8a)andtheSIvalue(-0.97)withrespecttogypsum(Fig.11c)inthehighly mineralizedwatersfromwellS49(ofCa-SO4watertype)showadissolutionofgypsum.Thisisobservedinmangrovesoil, andwouldreleaseCa2+andSO
42−intothegroundwater(Eq.(1)).Otherwise,consideringthelowpH(3–5),theenrichment ofSO42−mayalsoresultfrompyriteoxidation(Eq.(2)),usuallyoccuringinmangrovedegradationsoils(LebigreandMarius, 1984;Kristensenetal.,1991) CaSO4⇔Ca2++SO2−4 (1) FeS2+ 7 2O2+H2O⇒CO2+⇔CH2CO3⇔F 2+ e +2S024−+2H+ (2)
b)Group2isrepresentedbywellsamplesS3,S4,S5,S18,S19,S20,S21,S24,S26,S28,S29andS33,locatedintheeastern partoftheregion,andbysampleS48(Fig.10),locatedinthecoastalstrip.SampleS48characteristicsdifferfromother samplesingroup2inthatitexhibitshighvaluesofCl−(870mg/L)andNa+(324.3mg/L)andisaNa-Clfacies.ItsECvalues varyseasonally(3430and239S/cmduringthedryandrainyseasons,respectively).Itissuggestingthatthiswelltapsthe
N.M.Diengetal./JournalofHydrology:RegionalStudies9(2017)163–182 175
Fig.9.Piper’sdiagramshowingtherelativechemicalcompositionsofgroundwater,SaloumRiverwaterandseawatersamplescollectedduringthe2012
dryseason.GroundwatersamplesbelongingtothethreegroupsdefinedwiththeSOMsmethodareplottedwithdifferentcolors.
Table3
SummaryofstatisticalhydrochemicaldataoffieldcampaignscorrespondingtodryandwetseasonsforgroundwatergroupsobtainedwiththeSOMs
analysis. Parameters CE T pH Ca2+ Mg2 Na+ K+ HCO 3- Cl- SO42- NO3 -S/cm) ◦C mg/l Dry 1 min 419 28.2 3.7 19 3 25 0.6 1.9 32.7 0.8 5 max 2191 30.3 6.2 124 14 98.1 58.7 161.9 187.3 426 296.7 median 730 29 5.5 43.9 6.3 58.4 3.6 25.6 110.1 3.5 66.3 average 872 29.1 5.5 50.8 9.7 62.1 8.6 48.0 110.7 39.5 100.7 2 min 268 27.7 6.2 39.1 0.9 5.2 0.7 100 5.7 0.1 0.1 max 1160 30 7 116.4 17 41 9.3 332.9 191 3.8 24 median 490 29.5 6.5 54.5 4.5 13.9 1.8 170.3 23.5 1.8 4 average 533.4 29.5 6.5 62.3 5.5 17.7 2.5 184.7 40 1.9 7.8 3 min 74.4 28 4.4 3.2 0.2 3.9 0.1 3.8 2.9 0.1 0.3 max 342 30.9 5.9 19.3 3.2 34.9 6.1 58.5 31.6 9.5 72 median 185 29.5 5.35 8.8 1.2 13.9 0.5 21.4 12.5 0.5 23.5 average 197 29.5 5.3 10 1.5 15.6 0.9 24.3 16.7 1.0 25.9 wet 1 min 388 26.4 4.6 31.9 4.3 28.5 9 6.5 33.9 1.5 6.9 max 2040 30 8.4 213.7 52.8 138.5 45.8 169.2 390.1 582.1 314 median 890 29 7.4 53.8 11.2 62.8 4 60.8 139.9 3.131 67.3 average 948.2 29.0 7 79.3 14.8 74.3 10.0 65.7 157.8 50.9 113.7 2 min 194 29.2 7 43.5 0.7 7.6 0.6 81.1 8.1 0.5 3.1 max 748 30.8 8.1 108.7 9.2 30.7 5 314.9 72.2 5.3 29 median 325 30.1 7.6 54.9 3.8 14.1 2.0 169.6 21.1 1.8 8.0 average 395.6 30.2 7.6 59.3 4.4 15.8 2.2 179.7 26.7 2.3 10.7 3 min 47 28.3 6.2 5 0.3 3.8 0.05 9.7 3.5 0.6 3.4 max 332 31.1 8.8 30.8 3.3 35.5 7.3 59.7 46.2 5.3 22.3 median 197 30.2 7.8 13.3 1.8 14.5 0.5 24.4 23.3 0.9 24.0 average 180.2 30.2 7.8 14.2 1.8 17.0 1.0 27.5 21.3 1.4 30.7
176 N.M.Diengetal./JournalofHydrology:RegionalStudies9(2017)163–182
Fig.10.Spatialdistribution,duringthe2012dryseason,ofthethreegroundwatergroupsasobtainedwiththeSOMsanalysis.
Fig.11.Relationshipbetweenthecontentsofa)Na/ClvsCl,b)[(Ca+Mg)-(SO4+HCO3)]vs[(Na+Cl)-(Cl+NO3)]andc)saturationindexvalueinthe ground-watersamplescollectedduringthe2012dryseason.ThethreedistinctgroupsarethosedefinedwiththeSOMsmethod.
N.M.Diengetal./JournalofHydrology:RegionalStudies9(2017)163–182 177 Table4
Summaryofstatisticalhydrochemicaldataoffieldcampaignsduringthewetseasonsof2003and2012forgroundwatergroupsobtainedwiththeSOMs analysis. Parameters CE Ca2+ Mg2 Na+ K+ HCO 3- Cl- SO42- NO3 -S/cm) mg/l 2003 1 Mean 2099.4 133.7 37.9 278.6 16.5 82.4 513.4 64.8 131.6 Median 1769.0 140.4 29.5 202.6 8.8 61.0 386.3 12.6 59.6 Min 1013.0 98.1 6.5 114.5 1.9 30.5 174.0 0.5 2.0 Max 4920.0 189.8 106.2 791.7 61.8 158.6 1498.0 368.0 259 2 Mean 486.0 41.8 4.0 48.6 1.3 134.2 88.9 4.0 10.0 Median 358.0 46.1 3.5 21.4 1.2 134.2 23.1 0.9 7.8 Min 35.0 5.3 0.2 2.9 0.6 39.6 1.5 0.2 1.6 Max 1686.0 50.0 6.2 234.0 2.6 225.7 75.3 23.6 29.2 3 Mean 216.0 16.8 3.7 20.2 2.6 58.0 20.5 1.0 49.0 Median 172.5 11.6 1.9 14.7 0.8 47.3 19.6 0.3 26.7 Min 62.0 3.8 0.2 6.8 0.1 27.4 2.6 0.1 5.9 Max 299.0 56.5 17.6 37.1 19.3 131.1 30.8 5.0 199.6 2012 1 Mean 1250.6 96.0 20.7 90.3 19.8 46.2 194.4 132 124.9 Median 1260.0 99.6 16.8 101.3 6.5 23.8 194.2 9.9 78.8 Min 360.0 30.0 4.3 19.3 0.9 7.6 58.4 1.7 32.1 Max 2191.0 213.0 52.8 138.5 45.8 91.1 390.0 582.4 200.1 2 Mean 365.0 54.1 3.1 15.1 2.2 150.7 30.2 2.5 9.7 Median 313.0 59.4 2.9 13.8 2 183.2 26.7 1.8 9.3 Min 194.0 30.7 0.3 5.9 0.6 34.1 64.5 0.8 0.5 Max 575.0 71.7 6.7 33.3 5.0 222.1 8.1 5.0 22.3 3 Mean 170.5 11.6 1.8 17.3 1.3 27.1 19.6 0.7 29.6 Median 161.0 10.7 1.4 14.9 0.6 25.7 18.3 0.7 20.6 Min 47.0 5.0 0.3 3.8 0.1 9.7 3.5 0.9 3.4 Max 286.0 18.7 3.9 37.5 7.3 49.9 34.0 1.0 86.8
dynamicseawaterinterfacecharacterizedbyseawateradvanceduringdryseasonfollowedseawardinterfaceretreatduring
rainyseason(i.e.whengroundwaterheadsarehigher).AttheexceptionofS48,thisgroupischaracterizedbyhighCa2+and
HCO3−contents,relativelylowCl−andNa+contentsandvariablemineralizationrangingfrom268to1160S/cmwithan
averageof533S/cmduringthedryseason.Thisgroupisfeaturedbyfreshanduncontaminatedgroundwaterthatisnearly
freeofmarinewatercontamination,andthegroundwaterfaciesaredominantlyCa–HCO3.ComputedSIvalueswithrespect
tocalcite(rangingbetween−1.7and0.7)anddolomite(rangingbetween−4and0.6)(Fig.11c),andCa/HCO3molarratios
(1)inadditiontooccurrenceofcalcitemineralinthereservoirmatrix(asevidencedbyLappartient,1985)reflectcarbonate mineralsdissolution.Thisreactionisthemaingeochemicalprocesswhichwouldbeconcomitanttoionexchangeinwhich Ca2+replacesNa+intheclaymatrix(Fig.11a).
c)Group3,whichisrepresentedbywellsamplesS6,S17,S25,S27,S30,S32,S39,S40,S41,S43,S44,S45,S46,S47,S50, S51,S53,andS64,ischaracterizedbylowmineralizedgroundwater.TheECvaluesarerangedfrom74.4to342S/cmin thedryseason.Morethan70%ofthesamplesexhibitlowECvalues(below250S/cm)suggestingalowermineralisation andtheirwatertypesaredominantlyNa–HCO3(33%),Na–Cl(33%),Ca–HCO3(22%)andCa–Cl(12%).Thesecharacteristicsof lowmineralisationandvariouswatertypeslikelydepicttherecentlyinfiltrationrainwaters.Theyarereachingtheaquifer accompaniedbybothrapidcation(NaforCa)andanion(ClforHCO3)exchangesintheclaymatrixoftheaquiferreservoir inadditiontocalcitedissolution.Thiswouldresultinaconsistentgroundwater-typegradationoflowmineralisedCa-Cland Na-HCO3typesevolvingtoNa-Cl,Ca-HCO3toCa-ClandNa-Clindicatingchangesalonggroundwaterflowpathsinthese zones(Mercado,1985;Hidalgoetal.,1995).
4.4. Interannualvariationsofgroundwatersalinitybetween2003and2012
Thetemporaltrendvariationsofgroundwatersalinitywereinvestigatedusingdatacollectedin2003and2012.Intotal, 28chemicalanalyseswereretrievedfromNovember2003(Fayeetal.,2004)andNovember2012(thiswork)asacomparison todepictchangesrelatedtoanthropogenicandnaturalstressinthisvulnerablesystem.SalinitypatternsoftheSaloumRiver waterECexhibitschangesfrom78,300to90,100S/cmin2003andfrom50,800to60,400S/cmin2012.Thesechanges muchlikelyderivefromrainfalleventswhichvariedfrom535mm(502.9mmeffectiverainfall)in2003–847mm(796.18mm effectiverainfall)in2012.Comparedwiththelong-term(1960–1990)averageof610mm,consideredasreferenceinSahel, the2003and2012rainfallrecordsrepresentrespectivelyadeclineof12%andanincreaseof38%.
Thishighvariationinrainfallbetweenthese2referenceyearswouldprobablyalsochangechemicalpatternsinthe groundwater.SOMsanalysesofthedifferentgroupsrevealed:
-InwellsS1,S2,S27,S34,S35andS38,whicharegenerallylocatedneartheSaloumRiverandcorrespondtothegroup 1intheSOMsanalysis,theECevolutionshowsadecreasingtrendwithvalueshigherin2003(averageofapproximately 2099S/cm)thanin2012(1250S/cm)(Table4).Theioniccontentschanges,showninthePiperdiagram(Fig.12),are featuredbyashiftofthegroundwatertypesfromNa-CltoCa-ClorCa-HCO3.ThisconfirmstheenrichmentofCarelative
178 N.M.Diengetal./JournalofHydrology:RegionalStudies9(2017)163–182
Fig.12.Comparisonofboxplotdiagramsasobtainedfora)majorionscompositionandb)electricalconductivity(EC)inCTgroundwaterbetweenwet
seasonsof2003and2012.
toNa,andthereforethesofteningbydilutioninferredbyinflowsofbothinfiltratedrainfallandSaloumRivercomparedto 2003(seeabove).
-InwellsS3,S19,S21,S22,S23,andS62,locatedinthecentralandeasternzonesmostly,andcorrespondingtogroup 2intheSOMsanalysis,theECvaluesincreasedfrom2003(meanvalueof353S/cm)to2012(averageofapproximately 587S/cm).ThisisalsoobservedintheioniccontentsofthegroundwatersamplesasconfirmedbythePiperdiagram(Fig.13). GroundwatertypesmostlyevolvedfromCa-HCO3toNa-ClorCa-Cl.Thesecharacteristicsofincreasedmineralisationand enrichmentofHCO3-,Cl−and/orNO3−insomewellslikelydepicttherecentlyinfiltrationrainwaters.Itisreachingthe aquiferaccompaniedbybothcombinedcalcitedissolutionandpollutantsfromanthropiccontamination.
-NearthecoastandtheNemaRiver,notrendcanbedistinguished.TheECvaluesdecreasedinsomeofthewells(e.g., S40,S41,S48,andS50)(from1750toapproximately200S/cm)andincreasedinothers(e.g.,S42,S49,andS52)(from 974toapproximately1539S/cm).Inthisregion,thechemicalevolutionofthegroundwaterwasduetoacombinationof seawaterintrusionthatwasenhancedbypumpingactivitiesanddilutionbyrecharge.
4.5. Isotopecomposition
Often,isotopicresultsgreatlyhelpforunderstandingthestructuralcontrolsongroundwaterflowinaridregions(e.g. Daileyetal.,2015)andtherechargepatterns(amongmanyothers:ShahulHameedetal.,2015).Here,theresultsoftheisotope analysesofthesurfacewaterandgroundwatersamplesarepresentedinTable1.Isotopicanalyseswereonlyperformed onasubsetofsamplesthatwerecollectedinNovember2012,whichcorrespondstotheendoftherainyseason.The␦18O and␦2HvaluesofthegroundwatersamplesandtheSaloumRiverwaterareplottedagainsttheGlobalMeteoricWater Line(GMWL)andtheLocalMeteoricWaterLine(LMWL)ofequation(␦2H=7.93␦18O+10.09)definedbyTravietal.(1987) (Fig.14a).
TheSaloumRiversamplesaredistinctlyenrichedwithvaluesrangingfrom−0.11to+0.32‰for␦18Oandfrom−5.4to −3.2‰for␦2H.ThesesamplesdeviatesignificantlyfromtheSMOWvalues(Fig.14a)confirmingprominentevaporation processesaffectthelowtostagnantSaloumRiverwater.Inthegroundwatersamples,the␦18Ovaluesrangefrom−5.4to −4.1‰,andthe␦2Hvaluesrangefrom−36to−31‰,withmeanvaluesof−4.9‰and−33‰,respectively.Plottedinthe ␦2Hvs.␦18Odiagram,thedataclusterbelowtheLWMLalongtheline␦2H=3.9␦18O−14.3(R2=0.83).Thesamplesplotto therightoftheglobalmeteoricindicatesanenrichmentofheavyisotopes,andsuggeststhattheyweresubjectedtovariable degreesofevaporation
Indeed, in the Saloum environment, where temperatures (mean 28,5◦C) are high as well as evapotranspiration (2030mm/year),itislikelythatrechargewaterfromrainfallevaporatesbeforeand/orduringafterinfiltration.
Twodistinctclusterscanbedistinguishedinthegroundwatersamplesusingtheisotopicdata(Fig.14a).InclusterA,the stableisotopevaluesrangefrom−5to−4.1%for␦18Oandfrom−35to−31%for␦2H.Thisclusterrepresentssamplesofgroup
N.M.Diengetal./JournalofHydrology:RegionalStudies9(2017)163–182 179
Fig.13. Piperdiagramshowinggroundwatercompositionchangebetweenwetseasonsof2003and2012.
1,whicharelocatedalongthecoastandneartheSaloumRiver.ClusterBischaracterizedbymoredepletedstableisotope valueswith␦18Orangingfrom−5.4to−5.1%and␦2Hrangingfrom−36to−34%.Thisclusterrepresentsfreshgroundwater samplesofgroups2and3.ThegroundwaterofclusterAappearstobemoreaffectedbyevaporationorismoreinfluencedby theintrusionofevaporatedsurfacewater.Bycomparing␦18OandCl−(Fig.14b),theexistenceofthetwopreviousclusters isconfirmed.ThesamplesofclusterAarelocatedonamixinglinethatjoinsthesamplesofclusterB,whichrepresentfresh water,andthesamplesfromtheSaloumRiverandtheocean.ThisconfirmsthatthesalinizationofthesamplesofclusterA iscausedbymixingwithcoastalmarineorSaloumRiverwaters.
TheresultssuggestedthattheCTaquiferintheinvestigatedareashavebeenrechargedby
rainwaterinfiltrationandmixedwithsalinesurfacewaterfromtheSaloumRiver,whichisalsoaffectedbyhigh evapo-rationprocesses.Fayeetal.(2004)hypothesizedfiveprocessesmayleadtothisscatteredpattern:1)mixingprocessalong flowpathscombinedwithevaporationfromtheshallowwatertable;bothcanhomogenisethe␦18Ovaluesandincrease theoverallsalinity;(2)theisotopiccontentsofrechargedwatersandtheSaloumRiverwatercanhaveawiderangeand alsohomogenizationof␦18Ovalues;(3)transpirationfromvegetationcover;(4)dissolutionofthesaltmineralsmayleadto changingboththeSaloumRiverhydrochemistryaswellastheinterstitialwaterchemistryincreasingthereforesalinityin thetransitionzone;(5)toalesserextent,thesaltsecretinghalophytesplantsofthemangrovesystemlocatedatthemouth oftheestuarymayleadtotheenrichmentofsalinityintheunsaturatedzonewithoutisotopicfractionation.
AsshowninFig.14c,theSaloumRiverwasnotablydepletedinheavyisotopesinNovember2012incomparisonto November2003,whichvaluesrangefrom1.5to1.7‰for␦18Oandfrom0to3‰for␦2H.Otherwise,theevaporatedtrend ofthe2003groundwatersamplesdeviatesmoresignificantly(slopeof3.9)fromtheLMWLthanthoseofthe2012samples (slopeof4.9)(Fig.14c).TheseresultssuggestthedilutionoftheSaloumRiverwaterandthefresheningofgroundwaternear theriverduetotheincreasingamountoffreshwaterfromrainfallbetween2003and2012(Fig.14c).
5. Conclusions
TheCTaquiferrepresentsanimportantgroundwaterresourceinSenegalandparticularlyintheSaloumregion,whereit isthemainsourceofdrinkingwaterforthelocalpopulation.Therefore,thereassessmentofprocessesresponsibleforthe observedmineralizationanddegradedwaterqualityandofthegroundwaterqualitychangesoftheCTaquiferisofgreat importance.Thisreassessmentmustbedoneinthelightofthenewconstraints(e.g.changesinclimaticconditionsand pumpingconstraints),andthenewflowpatternconfigurationinthissystem.Thesimultaneousanalysisofhydrogeochemical and isotopicdatausingconventionalandstatisticalmethods allowstheassessmentofthegroundwaterquality inthe
180 N.M.Diengetal./JournalofHydrology:RegionalStudies9(2017)163–182
Fig.14.Relationshipbetweena)␦2Hand␦18Oandb)␦18OandClintheCTgroundwaterduringthe2012wetseasonandc)␦2Hand␦18OintheCT
groundwaterduringthewetseasonsof2003and2012.ThegroundwatersamplesareclassifiedusingthethreegroupsdefinedwiththeSOM’smethod.
southernpartoftheSaloumBasin.Statisticalanalysesofthegeochemicaldatademonstratethespatialvariabilityofthe chemicalcharacteristicsofthegroundwater.Theyallowtodistinguishthreegroupsofgroundwater.Thefirstgroup(1),which islocatednearthecoastandneartheSaloumRiver,isaffectedbymixingwithsalinewaterintrusionand/oranthropogenic pollution,andthemainfaciesareNa-ClorCa-Cltypes.Thesecondgroup(2),whichismainlylocatedinthecentralandeastern partsofthestudyarea,islessmineralizedandcontainsCa-HCO3faciesasaresultofcalcitedissolutionduetointeraction withtheaquifer.Inthethirdintermediarygroup(3),somesamplesindicatedfresheningprocesseslikelydepictingtheeffect ofrecentinfiltrationrainwaters.
Thesethreegroupsandtheirchemicalcharacteristicsaregenerallyobservedinboththedryandwetseasons.However, adecreaseofthemineralizationisgenerallyobservedduringthewetseasonduetotherechargeoflessmineralizedwater. Acomparisonofthegroundwaterqualitycharacteristicsintermsofsalinizationbetween2003and2012indicatesthat significantchangeshaveoccurred.InthewellsthatarelocatedneartheSaloumRiver,decreasesoftheNa+andCl- concen-trationsandtheECvaluesareobserved.ThegroundwaterfacieshavegenerallyevolvedfromNa-CltoCa-ClorCa-HCO3, whichindicatesthedilutionofgroundwaterduetofresheninginthevicinityoftheSaloumRiver.Thisfresheningisdueto anincreaseofrainfallaswellastheintrusionoflessmineralizedwaterinrecentyearsasthesalinityoftheSaloumRiver hasalsodecreased.Anincreaseofmineralizationisobservedinsomewellslocatedinthecentralandeasternzonesofthe studyarea.GroundwatertypesmostlyevolvedfromCa-HCO3toNa-ClorCa-Clandindicaterecentinfiltrationrainwaters reachingtheaquiferaccompaniedbybothcombinedcalcitedissolutionandpollutantsfromanthropiccontamination.No trendcanbedistinguishednearthecoastandtheNemaRiverwherethechemicalevolutionofthegroundwaterwasdueto acombinationofseawaterintrusionanddilutionbyrecharge.
Insummary,changesofgroundwaterlevelsandqualityhavebeenobservedintheCTaquiferbetween2003and2012 inresponsetovariationsintheprecipitationregimeandotherfactors.Additionalchangesinrechargeorintheflowregime willoccurinthenearfutureinresponsetoclimatechangeortoincreasesofgroundwaterpumping.Itisthusimportant toidentifytheevolutionofthegroundwaterqualitythatiscausedbythesenewchangestoavoidormitigatethefuture degradationofgroundwaterqualitybeforeitbecomesamajorobstacletothefutureeconomicdevelopmentofthiscoastal area.
N.M.Diengetal./JournalofHydrology:RegionalStudies9(2017)163–182 181
Acknowledgments
TheauthorsthanktheInternationalFoundationofSciences,FrancophoneUniversityAgencyandtheANGLEprojectfor financialsupporttocarryoutthiswork.TheyalsothanktheHydrogeologyLaboratoryoftheUniversityofLiège<(Belgium), theDepartmentofGeologyofCheikhAntaDiopUniversityinDakar(Senegal)andtheHelmholtzZentrumMünchen,Institute ofGroundwaterEcology(Neuherberg/Germany).Theauthorsaregratefultothetwoanonymousreviewerswhohelpeda lotforimprovingthepaper.
AppendixA. Supplementarydata
Supplementary data associated with this article can be found, in the online version, at http://dx.doi.org/10.1016/j.ejrh.2016.12.082.
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