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SUPPLEMENTARY INFORMATIONDOI: 10.1038/NCLIMATE3085
NATURE CLIMATE CHANGE | www.nature.com/natureclimatechange 1 1
Climate change unlikely to increase malaria burden in West AfricaSupplementaryInformation
SupplementaryMethods
EnvironmentaldatainputsforHYDREMATSsimulations
EnvironmentaldatainputsusedforthisstudyaresummarizedinSupplementary
Table4.Weusedhigh-resolutionsatelliteobservationsofrainfallfromtheClimate
PredictionCenterMorphingTechnique(CMORPH)Version1.0dataset,whichgives
~8kmresolutionrainfalldataevery30minutes1,andhasbeenfoundinmultiple
comparisonstudiestobeoneofthemostskilledsatelliterainfallproductscurrently
available2.CMORPHdataiscreatedbycombiningimagesfrommultiplepassive
microwavesensors,andinterpolatingthemforwardandbackwardinspaceand
timebasedoncloudadvectionvectorscalculatedfromgeostationaryinfrared
sensors1.
Likemostsatelliteproducts,CMORPHisknowntohaveapositivebiascomparedto
raingaugedatainWestAfrica,primarilyduetooverestimationofhigh-intensity
rainfall3.However,afterasimplebiascorrection,CMORPHcanbeusedasaninput
toHYDREMATStoaccuratelysimulatethehydrologicalvariablesrelevanttomalaria
transmission4.Weusedaprobabilitymatchingtechnique5sothatthecumulative
distributionfunction(CDF)ofcorrectedhourlyCMORPHdatamatchedthatofthe
groundobservations.Variationsofthistechniquehaverecentlybeenusedto
correctbiasesinCMORPHusingraingaugedata6,7.
Wedownloadedtemperature,windspeed,winddirection,andradiationdataforthe
HYDREMATSsimulationsfromtheERAInterimdataset8(downloadedfrom
http://www.ecmwf.int/en/research/climate-reanalysis/era-interim).Weassumed
uniformclimaticconditionswithinthe0.75degreeERAgridcell.Weconverted
ERA-interimwindspeeddatafroma10-meterelevationtoa2-meterelevationfor
useinHYDREMATSbyusingalogarithmicprofile.Also,welinearlyinterpolatedthe
Climate change unlikely to increase malaria burden in West Africa
© 2016 Macmillan Publishers Limited. All rights reserved.
2
ERA-Interimdatafromtheprovided3-hourresolutiontoa1-hourresolutionas
requiredbyHYDREMATS.
WeassignedthedominantvegetationtypeateachlocationusingtheUniversityof
MarylandLandCoverClassification9,andassignedsoilpropertiesusingthe
HarmonizedWorldSoilDatabase10.Werepresentsoilcrustinginthemodelusinga
thinlayeroflow-permeabilitysoilasistypicalinWestAfricaundercultivated
conditions11.Becausethisstudyfocusesonclimatevariables,weheldtopography
constantbetweenlocationsandassumedthatBanizoumbou,Nigertopography
representstypicaltopographicalconditionsandhousingpatternsintheWestAfrica
Sahel12.
Downscalingandbiascorrectionofclimatechangeprojections
ThemethodologythatweusetodownscaleGCMspredictionsofchangesinrainfall
andtemperatureisbasedontwoassumptionsthatarerootedintheconclusionsof
previousstudies:
(A)TheGCMshavelimitedaccuracyinsimulatingthecurrentandfutureclimateof
WestAfrica13-15.InparticulartheGCMshavepooraccuracyinsimulatingthe
temporalpatternsofrainfallatthedailytimescale16.Asaresult,weonlyusethe
GCMssimulationstoextractinformationaboutfuturechangesin(i)annualrainfall
magnitude;andin(ii)seasonaldistributionoftemperature;
(B)Thetemporalrainfallpatterns,attimescalesfromminutestoweeks,are
criticallyimportanttotheformationofthewaterpools,themainbreedingsitesfor
mosquitos17.Thephysicalandbiologicalrelationshipsthatshapepoolformation,
andmosquitopopulationdynamicsarehighlynon-linear.Itisnottrivialhowto
averagethesestronglynon-linearrelationshipsformsmallscales(1hour,10m)to
© 2016 Macmillan Publishers Limited. All rights reserved.
3
largescales(months,10kilometers)18.Thisiswhyinthesimulationspresentedin
thispaper,ourmalariatransmissionsimulationsarecarriedattheresolutionsof1
hour,10meters.Asaresult,thepatternsofrainfallusedtoforcethemodelhastobe
realistic,consistentwithobservations,andwecannotsimplyusethetypically
erroneoustemporalpatternssimulatedbyclimatemodels.
Basedontheseassumptionsanddiscussion,weapplythefollowingmethodologyin
describingtheforcingofoursimulations:
(1)Themagnitudeoftheaveragechangeindailytemperatureisestimatedfromthe
GCMsimulationsforeachmonthoftheyearandforeachlocation(x1,y1).This
estimatedchangeisthenaddeduniformlytotheobservedtimeseriesfromERA
interimreanalysisdataset,with3-hourtemporalresolutionand2.5degreesspatial
resolution,at(x1,y1),asastraightforwarddeltamethodapproach19-21.The
resultingtimeseriesisusedtorepresentthefuturetemperatureat(x1,y1).
(2)Therelativechangeinmagnitudeoftheannualrainfall,underfutureclimate
conditions,isestimatedfromtheGCMsimulationsforeachlocation(x1,y1).This
relativechangeismultipliedbytheactualobservedannualrainfallat(x1,y1),in
ordertoestimatetheprojectedfutureannualrainfallat(x1,y1).Asavariationon
thedeltamethod,ratherthanmultiplyingourdailyorhourlyprecipitationtime
seriesbythedeltavalue,weinsteadchosetheclosestlocation(x1,y2)wherethe
annualrainfallunderthecurrentclimate,basedonobservedsatellitedatathathas8
kmresolution,isequaltotheprojectedfuturerainfallat(x1,y1)isidentified.The
satellite-basedtimeseries,at30minutesresolution,at(x1,y2)isassumedto
representthefuturerainfalltimeseriesatlocation(x1,y1).Formostcases,(x1,y2)
islocatedwithinabout100kilometersnorthorsouthof(x1,y1),ie.withinthesame
ERAinterimgridpoint.
ThisapproachhastheadvantageofremovingGCMbias,whileretainingfine-scale
spatialandtemporalvariabilityofhistoricalrainfallandtemperature19.The
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disadvantageisthatthemethoddoesnotaccountforchangesinrainfalland
temperaturedistributionsaroundthemean.Thismaybeproblematic,especiallyin
thecaseofextremeeventssuchasfloodsordroughts,whichareimportantfor
waterpoolformation,andveryhightemperatures,whichaffectmosquitosurvival.
ThismethodalsoneglectschangestotheWestAfricanmonsoon,whichhavebeen
showninrecentstudiestooccurinclimatemodelsasaresultofseveralcompeting
physicalresponsestoclimatechangeincludinganenhancedconvectivebarrierin
thepre-monsoonmonths,enhancedmonsoonflowduetogreaterdifferentialin
land-seatemperatures,andvegetationfeedbacks22-25.Theeffectsofthese
mechanismsleadtoprojecteddecreasesinrainfallduringthemonsoononset,
followedbyincreasedprecipitationlaterinthewetseason22-25.Thetimingofthe
switchbetweenthenegativetopositiverainfallanomalywasshowntodetermine
theoverallchangestototalrainfallandlengthofrainyseason,andremainshighly
uncertain23.Sucheffectscanimpactmalariatransmission,particularlyiftheyalter
thedurationoftherainyseason,asthiswouldinturnalterthelengthofthemalaria
transmissionseason.Changestothefrequencyandintensityofrainfallevents
withintherainyseasoncouldalsohaveimportantimpacts,astheseaffectwater
poolpersistenceandplayalargeroleindeterminingthemalariaresponseto
rainfall17.
© 2016 Macmillan Publishers Limited. All rights reserved.
5
SupplementaryDiscussion
Comparisonofsimulatedvariablestoobservationaldata
HYDREMATShaspreviouslyundergoneextensivevalidationintwovillagesin
SouthernNiger26-28.Datasamplinglocationsinoneofthevillages,Banizoumbou,
areshowninSupplementaryFig.2.Environmentaldatacollectedincludedone-
hourresolutionmeteorologicalvariables,spatiallydistributedsoil,vegetationand
topographyvalues,andtime-varyingmeasurementsofsoilmoisture,andthedepths
andtemperaturesofselectedrecurringwaterpools.Entomologicalvariables
collectedincludedadultmosquitoescapturedinCDClighttrapsandmosquito
larvaecollectedusingastandarddippingmethod26,27.Bimonthlybloodsamples
weretakenfromchildrenagedonethroughfiveyearsold28.Wedemonstratedthe
model’sabilitytosimulatehydrology,entomologyandmalariaprevalenceinthis
region26-28.
Here,wepresentadditionalmodelvalidation,throughacomparisonofsimulations
toobservationsfromthreeothersources:theBeierdatasetonEIRandmalaria
prevalence29,malariaprevalenceestimatesfromtheMalariaAtlasProject30,and
entomologyandmalariaprevalencedatafromtheGarkidistrictinNigeria31.
ComparisontoBeierdata
Beieretal.29compiledpaireddatafrom31locationsacrossAfricaanddevelopeda
relationshipbetweentheentomologicalinoculationrate(EIR),andmalaria
prevalence.Thesepaireddatapointsoriginatedfrommultiplecountriesincluding
Kenya,Ethiopia,Tanzania,RepublicofCongo,BurkinaFaso,andSenegal,spanninga
widerangeofclimatezones.Thepaireddatapointswereselectedbyconductinga
literaturesearchwiththefollowinginclusioncriteria:entomologicaldatacollected
overatleastoneyearwithaminimumofmonthlysamplingoverthetransmission
season,standardmethodsforestimatingmosquitodensitiesandsporozoiterates,
andnovectorcontrolinterventions.Inclusioncriteriafortheprevalencedata
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includeduseofstandardbloodsmeartechniquesandreportingbytimeperiodand
agegroup.Ininstanceswheretheoriginalmalariaprevalencedatawerereported
formultipletimeperiodsandagegroups,thesinglehighestprevalencevaluewas
selected.Theanalysisshowedalinearrelationshipbetweenprevalenceandthe
logarithmofannualEIR.Thislog-linearrelationshippersistedwhendatawere
stratifiedbyecologicalzoneaswellasbetweenEastandWestAfrica,indicatingthat
thisisafundamentalrelationshipandindependentofclimate.Thesedatatherefore
provideatestforthehumanimmunityandmalariatransmissioncomponentof
HYDREMATS,whichhasbeenlessextensivelytestedagainstobservationsthanthe
hydrologyandentomologycomponents.
BecauseBeieretal.usedthemaximumprevalencevaluesampledovermultipleage
groupsandtimeperiods,wecomparedthedatatothemaximumsimulated
prevalenceforthe2to10yearagegroupfromourequilibriumsimulations.
HYDREMATSwasabletoreproducetheobservedlog-linearrelationshipbetween
EIRandpeakmalariaprevalence(Figure2,maintext).Oursimulationresultsand
observationaldataagreeverywellforawiderangeofepidemiologicalconditions,
from0toover300infectiousbitesperpersonperyear.
ComparisontodatafromtheMalariaAtlasProject
TheMalariaAtlasProject(MAP),basedattheUniversityofOxford,producesmaps
showingglobalestimatesofvariousmeasuresofmalariarisk.MAPcompilesand
maintainsadatabaseofroutinemalariaprevalencesurveys.Thecurrentmapsuse
over22,000geo-referenceddatapointsofmalariaprevalencemeasuredbetween
1985and2010fromacrossthe85malariaendemicnationsandstandardizedtothe
2to10yearoldagegroup30.Temperatureandariditymasksareusedtopredictthe
limitsofstablemalaria.Withinthepredictedlimitsofstablemalariatransmission,
theseprevalencedataaremappedtoaglobalsurfaceata5kmx5kmresolution
usingBayesianinferenceandgeospatialmodeling30.TheMAPestimateofmalaria
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prevalenceinchildrenaged2to10yearsisshownasthecoloredsurfacein
SupplementaryFig.3,toppanel.Thecolorsoftheoverlayingcirclesshowthe
prevalenceduringthepeakmalariatransmissionseasonsimulatedbyHYDREMATS
intheequilibriumsimulations.
SupplementaryFig.3,bottompanel,comparessimulatedpeakprevalencetothe
MAPestimate,withresultsoftheequilibriumsimulationontheright,andthemean
ofthemultiyearsimulationontheleft.Forthemajorityofthetwelvelocations,
simulatedresultsmatchwellwiththeMAPestimate.Oneoutlierintheequilibrium
resultsisthepointS1,locatedinSenegal.Thiscouldbeexplainedinpartby
Senegal’smalariacontrolactivities,whichcauseobservedprevalencetobe
substantiallylowerthanwhatwouldhavebeenexpectedgiventheenvironmental
conditions.Oursimulationsdidnotaccountforvaryinglevelsofmalariacontrol
betweenlocations.Inter-annualvariabilityislikelyplayingaroleaswell,asthe
MAPestimatesdonotaddressseasonalandinter-annualvariabilityinresponseto
climate.AnotherdiscrepancybetweensimulationsandMAPestimatesarethethree
locations(N1,N2andM3)wheresimulatedprevalencewas0%,whileMAP
estimateslevelsbetween10and30%.Thereareseveraladditionalexplanationsfor
thisdiscrepancy.OneisthatinthesparselypopulatedregionsofnorthernNiger
andMali,thereareveryfewobservationsofmalariaprevalence.Intheseregions,
MAPestimatesrelyonstatisticaltechniquesusingenvironmentalcovariates
includingrainfall,temperature,landcover,andruralversusurbanclassification.
WethereforehavelessconfidenceinMAPestimatesathighlatitudes.Another
explanationforthediscrepancyisthatwhiletheequilibriumsimulationpredicted
R0lessthanoneleadingtoeliminationoftheparasite,allthreeoftheselocations
hadatleastsomeyearswithR0greaterthanone.Transmissionisthereforepossible
intheselocationsiftheparasiteispresentinthepopulationduringyearswithR0
greaterthanone.Athirdpossibilityforthediscrepancyisthattheselocationsmay
havehadsomeformofpermanentwatersourcenotaccountedforinour
simulationsthatcouldserveasmosquitobreedinghabitatintheabsenceofrain-fed
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waterpools,suchasoases.ThisislikelytobetrueofM3,whichliesonthebanksof
atributarytotheNigerRiver.
ComparisontodatafromtheGarkiProject
TheGarkiProjectwasamajorefforttostudymalariatransmissionandcontrolby
theWorldHealthOrganizationandtheGovernmentofNigeriafrom1969to1976.
ThestudylocationcorrespondswithsiteNA1showninFig.1inthemaintext.The
goalsoftheprojectweretostudytheepidemiologyofmalariatransmissioninthe
SudanSavannaclimatezone,testinterventionmethods,anddevelopamodelof
diseasetransmission31.Thestudyincludedfourtiersofvillages.Malariacontrol
interventionswereappliedtotheinnervillages.Villagesoutsideoftheintervention
zoneweremonitoredasnon-interventioncomparisonlocations.Mosquitoeswere
capturedevery5weeksduringthedryseasonandevery2weeksduringthewet
seasonusinghumanlandingcatches.Humanbaitcollectorswerestationedat
indoorandoutdoorlocationsforthedurationofthenightandcollectedmosquitoes
attemptingabloodmeal.Mosquitoeswerealsocapturedusingpyrethrumspray
collectionsandlighttraps.Capturedmosquitoeswerecountedandanalyzedin
ordertoestimatethemosquitobitingrate,EIR,mosquitoage,andthesporozoite
rate(proportionofmosquitoesinfectedbytheplasmodiumparasite).Age-specific
malariaprevalencewasmeasuredforselectedvillagesevery10weeksusing
standardbloodsmearmethods.Seroimmunologicalsurveyswereconductedevery
6monthstotestforthepresenceofantibodiestoPlasmodiumfalciparumandother
formsofthemalariaparasitewithinthehumanpopulation.
SupplementaryFig.4showsacomparisonbetweendataonmosquitobitingrates
collectedfromKwaruvillageoutsideoftheinterventionareaandthecorresponding
variablesimulatedbyHYDREMATSinour15-yearbaselinesimulation.Becausethe
high-resolutionenvironmentaldatasourcesrequiredforHYDREMATSsimulations
didnotoverlapwiththeGarkiProjecttimeperiod,wecomparedtheresultstothe
rangeofvaluessimulatedinour15-yearsimulation.Asshowninthefigure,the
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modelreproducesthegeneralcharacteristicsandtimingoftheseasonalcycle.Our
simulationresultsshowmosquitobitingactivitytoberestrictedtotheperiod
betweenMayandearlyNovember,correspondingtotheavailabilityofrain-fed
waterpoolsrequiredformosquitobreeding.Theobservationsshowoccasional
mosquitobitesoutsideofthisperiod;thesemayhavebeenmosquitoesthathad
takenrefugeinsideofhomes,orwereengaginginlow-levellocalizedbreedingina
permanentwatersourcenotrepresentedinourmodel.Oursimulationsalso
includelowlevelsofmosquitoestosustainthemosquitopopulationoverthedry
season;however,thesemosquitoesareassumedtoenteranaestivationstateanddo
notengageinbloodseekingactivityuntilthebeginningofthefollowingwet
season32.
ThetoppanelinSupplementaryFig.5showsprevalencebyageforacross-section
ofthepopulationinthenon-interventionvillagesmeasuredinOctober,1971,atthe
endofrainyseason.Theobservations,inred,showacharacteristicageprofileof
malariaprevalence.Youngchildrenbecomeinfectedathighratesuntiltheybegin
todeveloppartialimmunitytodisease.Thisexplainsthesharpdecreasein
prevalencebetweenthefirstfewyearsoflifeandearlyadolescence.Whiletheexact
shapeandmagnitudeoftheprevalenceprofilevariesbyyearandbylocation,
HYDREMATSsucceedsinsimulatingthebasiccharacteristicsoftheageprofile.In
thissimulation,childrenappeartodevelopimmunityseveralyearsfasterthanthe
observedpopulation.
Finally,thebottompanelofSupplementaryFig.5showstheseasonalcycleof
malariaprevalenceintheGarkidistrict.Theredandbluelinesshowobserved
prevalencesampledintwonon-interventionvillagesoverfouryears(1971-1974),
andsimulatedprevalenceinthesameareabetween1998and2012.Whilethe
specificprevalencevaluevariesfromyeartoyear,HYDREMATScorrectlysimulates
thetimingoftheseasonalpeakaroundearlyOctober,andsimulatesreasonable
levelsofprevalence.
© 2016 Macmillan Publishers Limited. All rights reserved.
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Thesimulationsshowedmuchhigherinterannualvariabilitythantheobservations.
However,theobservationsspanonlyfouryears,withrelativelylowandstable
rainfall(between300-600mm/year).Bycontrast,meanannualrainfallbetween
1998-2012was765mm,withastandarddeviationof168mm,andasmuchas586
mmdifferencebetweenconsecutiveyears.Itisthereforenotunreasonablethatwe
shouldseesuchhighvariabilityinsimulatedmalariaprevalenceoverthistime.Our
simulationsalsotendtounderestimatemalariaprevalenceinthedryseason.One
possibleexplanationforthisisthatoursimulatedpopulationhadhigherimmunity
levelsthantheobservedpopulation,causinginfectionstoclearmorerapidly.There
wasalsoevidenceoflowlevelsofmalariatransmissionoccurringduringthedry
season,whichgenerallydidnotoccurinthemodelsimulations31.
Regressionrelationshipsbetweenclimateandmalariatransmissionindices
Wedevelopedalinearregressionmodelforeachofthemalariatransmission
indices.Webrokeannualrainfallintosegmentsthataccountedforthresholdeffects
andothernonlinearitiesbetweenrainfallandpredictorvariables.ForR0,theslope
oftheleast-squaresregressionlinewasgreaterforannualrainfallvalueslessthan
690mmthanitwasforhighervalues.Inyearswithrainfalllessthan690mm,
mosquitoeswereconstrainedbytheavailabilityandpersistenceofsufficiently
persistentdevelopmentalhabitats.Additionalrainfallmadeitmorelikelythata
waterpoolwilllastlongenoughforlarvaetoemergeasadults,thusincreasingR0.
Inyearswithheavyrainfall,mosquitoeshadmanywaterpoolsavailablefor
breeding,sotheabundancewaslesssensitivetoincreasesinrainfall.Excess
rainfallcanleadtopoolsthataretoodeepforAnophelesgambiaes.l.mosquitoes,
whichprefertobreedinshallowareas.Larvalmosquitoabundanceisalso
regulatedbythecarryingcapacityofdevelopmentalhabitatsinyearswithample
rainfallanddensity-dependentmortality.
© 2016 Macmillan Publishers Limited. All rights reserved.
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TherelationshipbetweenrainfallandEIRhadtwodistinctsegments.Rainfallwas
linearlycorrelatedtothelogarithmofEIRforannualrainfallupto950mm.Beyond
thisthreshold,thetwowerenolongercorrelated,bothbecauseofthewaning
influenceofrainfallonmosquitonumbersathighrainfall,andalsobecause
prevalencedidnotincreasewithrainfallbeyondthispoint.
Theinfluenceofrainfallonprevalenceandtheimmunityindexhadthreedistinct
segments.Forrainfallvalueslessthan415mmperyear,environmentaland
entomologicalconditionsweregenerallyinsufficienttosustaintransmission,
resultinginnear-zerovaluesofEIR.Therewasalooselinearrelationshipbetween
rainfallandmalariaindicesforannualtotalsbetween415mmand950mm.There
wasalmostnocorrelationbetweenrainfallgreaterthan950mmandmalaria
transmission,duetothefinitenumberofsusceptibleindividuals,theupperlimitof
acquiringimmunity,andthedecreasedsensitivityofmosquitoestohighlevelsof
rainfall.
Sensitivityofresultstoclimatechangeprojections
Weinvestigatedthesensitivityofourresultstothechoiceofclimatechange
projectionsby1)extendingourmodelingstudytoincludetwoadditionalGCMs:
CanESM2andMIROC5and2)demonstratinghowFig.4(maintext)canbeusedto
estimatethesensitivityofresultstodifferencesinclimateprojections
1)InadditiontothetwoGCMsusedinourstudy(CCSM4andMPI-ESM-MR),we
conductedsimulationsusingtwoadditionalGCMstoinvestigatethesensitivityof
ourresultstothechoiceofclimateprojection.Thefourmodelsshowageneral
patternofdryinginthewesternportionofourstudyarea,andwettinginthe
easternandsouthernareas(SupplementaryFig.7).Themagnitudeofthese
changes,aswellastheextentoftheareawithpredicteddrying,variesbymodel.
ThispatternofrainfallchangeisconsistentwithasubstantialmajorityofCMIP5
© 2016 Macmillan Publishers Limited. All rights reserved.
12
modelsandhasbeenidentifiedasarobustfeatureoffutureclimateinthisregion14,24,33,34.
Temperaturesgenerallyincreasemoreinthewestthanintheeast,consistentwith
thespatialextentofpredictedchangesinprecipitation(SupplementaryFig.8).The
four-modelmeanshowstemperatureincreasesbetween2.5and5.8degreesCelsius
ofourstudyarea.MIROC5andCCSM4aresubstantiallycoolerthanthemean,while
CanESM2projectstemperatureincreasesover8degreesCelsiusinthewestern
Sahel.
MIROC5isknowntoproduceoneofthecoolestandwettestprojectionsoverthe
Sahel(Subregionsiiandiii)withintheCMIP5ensemble;mostCMIP5models
projecthighertemperatures,andrainfallwithin30%ofcurrentvalues14.Inthis
regard,oursimulationsresultsfromMIROC5canbeseenasaworst-casescenarioin
termsofpotentialincreasesinmalariatransmission.Bycontrast,CanESM2showsa
considerablystrongerdryingandwarmingsignalthantheotherthreemodels.The
resultsofoursimulationsusingallfourclimatemodelsareshowninTable4.
2)Theuncertaintyinclimateprojectionswasamotivatingfactorinour
developmentoftherelationshipslinkingrainfallandtemperaturetomalaria
transmissionindices,whichusesimulationsdrivenbyoveronethousand
combinationsofannualclimatedatatoexploreawiderangeoftemperatureand
rainfallconditionsthatmaybeobservedinthisregion.Theresultingplotsshownin
Fig.4,aswellastheregressionequationsoutlinedintheSupplementarymaterials,
canbeusedtoestimatetheeffectsofdifferentclimatechangescenariosonmalaria
transmissionthroughoutthisregion.
InSupplementaryFig.10,weshowthecurrentandfuturevaluesofmeanannual
rainfallandwet-seasontemperature,superimposedonthescatterplotsofmalaria
transmissionindicesinrainfall-temperaturespaceshowninFig.4.Theyellow
pointsshowthecurrentclimate,andthegreenpointsshowthefutureclimateas
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13
projectedbyeachofourfourclimatemodels.Thesensitivityofourresultsto
climateprojectionscanbeestimatedbyconsideringthespreadofthegreenpoints,
andthevaluesofRoandmalariaprevalenceintheunderlyingscatterplots.This
methodcanalsobeusedtoestimatetheclimatechangeimpactsonmalaria
transmissionforadditionallocationswithinstudyarea,aswellastheimpactsof
differentclimateprojections.Mostsignificantwouldbechangesthatcausethe
movementfromthehightransmission(red)tolowtransmission(blue)regionsof
rainfall-temperaturespace.Itisimportanttonotethatwhileeachlocationisshown
asasinglepoint,inrealitywewouldobserveacloudofpointssurroundingthe
meanduethehighinterannualvariabilityinrainfallandtemperature,asshownin
Fig.3band3c.
InSub-regioni,bothincreasedtemperatureanddecreasedrainfallworktoreduce
malariatransmission.Afutureclimatethatwassubstantiallywettercould
potentiallyleadtoincreasesinmalariaprevalence;however,suchafutureis
unlikelygiventhenear-consensusofcurrentgenerationclimatemodelsofadryer
futureinthisregion14.
InSub-regionii,anyfuturewarmingleadstoconditionsthatexceedthelimitsof
mosquitosurvival;noamountofadditionalrainfallcouldmakethisareasuitablefor
malariatransmission.
Asstatedinthemaintext,futuremalariatransmissionismostuncertaininSub-
regioniii,duetothecompetingforcesofincreasedmosquitobreedingthrough
higherrainfallandshortermosquitolifespanthroughincreasedtemperatures.
Furthermore,thisregionsitsclosetothethresholdofmalariatransmission;small
changescanpushthesysteminoroutoftheepidemicregion.Thisregionis
thereforethemostsensitivetotheselectionofclimateprojections.Inour
simulationresults,therelativelycoolandwetfuturepredictedbyMIROC5ledto
increasedprevalenceatsiteN2.
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14
Finally,Sub-region4iscurrentlydeepinthehigh-transmissionareaofrainfall-
temperaturespace.Modestchangesinclimatearenotsufficienttosignificantly
changefrequencyorseverityofepidemics.Howevertheverystrongdryingand
warmingsignalpredictedbyCanESM2wasenoughtocauseasignificantdecreasein
malariaprevalence.
© 2016 Macmillan Publishers Limited. All rights reserved.
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SupplementaryFigure1Schematicoftheprocesseslinkingclimatechangetomalariatransmission.Rainfallprimarilyaffectsmosquitobreeding,whiletemperatureaffectsmosquitolongevityandparasitedevelopmentrate.
© 2016 Macmillan Publishers Limited. All rights reserved.
16
Supplementary Figure 2 Data sampling locations in Banizoumbou, Niger. Reprinted from Bomblies et al26. The hydrology component of HYDREMATS was rigorously compared to field observations in Bomblies et al26, showing that the model very closely reproduced observed volumetric water content is soil, as well as location, depth and persistence of water pools.
© 2016 Macmillan Publishers Limited. All rights reserved.
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Supplementary Figure 3 Top: Malaria prevalence in children aged 2-10 in 2010 estimated by Malaria Atlas Project 30 (colored surface) and peak equilibrium prevalence simulated by HYDREMATS (colored circles). Bottom left: Simulated prevalence in children aged 2-10 for equilibrium simulation compared to MAP estimate. Each point refers to one of the twelve locations in the top panel. Bottom right: Simulated prevalence in children aged 2-10 over a 15-year simulation. Error bars on for the 15-year simulation show one standard deviation from the mean.
© 2016 Macmillan Publishers Limited. All rights reserved.
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Supplementary Figure 4 Mosquito biting rate in Kwaru, Nigeria, one of the non-intervention comparison villages in the Garki project31. Colored lines show captured mosquitoes for 3 consecutive years. Grey lines show simulation results.
© 2016 Macmillan Publishers Limited. All rights reserved.
19
Supplementary Figure 5 Top: Malaria prevalence by age group in October, 1971. The observations show that malaria prevalence peaks in childhood and gradually decreases through adolescence, with dramatically lower prevalence rates in adults. This is the result of semi-protective immunity, which is gradually acquired through repeated malaria infections. The blue bars show a cross-section of the simulated model population, showing a similar pattern of prevalence vs. age as older individuals are protected by higher levels of immunity. Bottom: Observed and simulated seasonal cycle of malaria prevalence in the Garki district. Grey lines show simulated malaria prevalence between 1998-2012. The red and blue lines show observed malaria prevalence sampled at two control villages over the period 1971-1974.
© 2016 Macmillan Publishers Limited. All rights reserved.
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Supplementary Figure 6 Mean annual rainfall [mm] during the period 1930-2005. The top-left panel shows observational data from CRU TS3.21. The remaining panels show rainfall simulated in the historical runs of the four climate models used in this study.
© 2016 Macmillan Publishers Limited. All rights reserved.
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Supplementary Figure 7 Predicted change in rainfall by 2070-2100 as a percentage of 1975-2005 mean rainfall under RCP8.5. Predictions are shown for the following CMIP5 models: CCSM4, MPI-ESM-MR, CanESM2 and MIROC5. The bottom-center plot shows the percent change averaged between CCSM4 and MPI-ESM-MR models, and the bottom-right plot shows the average prediction over all 4 CMIP5 models.
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Supplementary Figure 8 Predicted increase in July-August-September mean temperature between 1975-2005 and 2070-2100, in degrees Celsius, under RCP8.5. Predictions are shown for the following CMIP5 models: CCSM4, MPI-ESM-MR, CanESM2 and MIROC5. The bottom-center plot shows the percent change averaged between CCSM4 and MPI-ESM-MR models, and the bottom-right plot shows the average prediction over all 4 CMIP5 models.
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SupplementaryFigure9A)Thecolorsonthemapindicatesthechangesinaveragerainfallbetweencurrent(1975-2005)andfuture(2070-2100)conditions,averagingpredictionsbetweenthetwoclimatemodels.Thelabeledrectanglesgroupourstudyareabyresponsetoclimatechange.BandC)DetailedresultsforobservedchangesinR0andmalariaprevalenceareshownfortwosites,M7(Fig3Sb)inthesouthandN1(Fig.3SC)inthenorth.Thetoprowsshowlog10(R0)andthebottomrowshowsmalariameanprevalenceinchildrenaged2-10.Opencirclesindicatemodelresultsinthecurrentclimate,crossesshowresultswithfutureclimateconditionsaspredictedbyCCSM4andtrianglesindicateresultsusingclimatepredictionsfromMPI-ESM-MR.TheleftpanelsaremodelingresultsfromthedetailedHYDREMATSsimulations.TherightpanelsapplyaregressionrelationshiptoannualrainfallandmeanwetseasontemperaturedatafromCRUTS3.1.
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SupplementaryFigure10Migrationofstudysitesthroughrainfall-temperaturespaceunderdifferentprojectionsoffutureclimate.Thetriangularmarkersineachsubplotshowthelocationofastudysiteinrainfall-temperaturespaceundercurrent(yellow)andfuture(green)conditionsunderprojectionsfromfourclimatemodels:CCSM4,MPI-ESM-MR,CanESM2andMIROC5.Themarkersareoverlaidonplotsoflog(R0)(leftcolumn)andmalariaprevalenceinages2-10(rightcolumn).Thespreadbetweengreenmarkersestimatestheuncertaintyinfuturemalariatransmissionduetodifferencesinclimateprojections.
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Supplementary Table 1: HYDREMATS simulation results for baseline period (1975-2005) and future conditions (2070-2100). We show results for simulations using climate projections from the two GCMs selected for our study (CCSM4 and MPI-ESM-MR), as well as two additional models as a sensitivity analyses (CanESM2 and MIROC5). Red values indicate statistically significant decreases from baseline while green values indicate statistically significant increases. ProportionofyearswithR0>1(95%CI)
Sub-region Site Base CCSM4 MPI-ESM-MR CanESM MIROC5i M3 0.20(0.04,0.48) 0.00(0.00,0.22) 0.00(0.00,0.22) 0.00(0.00,0.22) 0.27(0.08,0.55)i S1 0.73(0.45,0.92) 0.27(0.08,0.55) 0.07(0.00,0.32) 0.00(0.00,0.22) 0.40(0.16,0.68)i M4 0.87(0.60,0.98) 0.53(0.27,0.79) 0.33(0.12,0.62) 0.00(0.00,0.22) 0.93(0.68,1.00)ii M1 0.00(0.00,0.22) 0.00(0.00,0.22) 0.00(0.00,0.22) 0.00(0.00,0.22) 0.00(0.00,0.22)ii M2 0.00(0.00,0.22) 0.00(0.00,0.22) 0.00(0.00,0.22) 0.00(0.00,0.22) 0.00(0.00,0.22)ii N1 0.13(0.02,0.40) 0.07(0.00,0.32) 0.00(0.00,0.22) 0.00(0.00,0.22) 0.00(0.00,0.22)iii N2 0.53(0.27,0.79) 0.67(0.38,0.88) 0.07(0.00,0.32) 0.40(0.16,0.68) 1.00(0.78,1.00)iii N3 1.00(0.78,1.00) 0.93(0.68,1.00) 0.33(0.12,0.62) 0.53(0.27,0.79) 1.00(0.78,1.00)iv M5 1.00(0.78,1.00) 1.00(0.78,1.00) 1.00(0.78,1.00) 1.00(0.78,1.00) 1.00(0.78,1.00)iv M6 1.00(0.78,1.00) 1.00(0.78,1.00) 1.00(0.78,1.00) 1.00(0.78,1.00) 1.00(0.78,1.00)iv NA1 1.00(0.78,1.00) 1.00(0.78,1.00) 1.00(0.78,1.00) 1.00(0.78,1.00) 1.00(0.78,1.00)iv M7 1.00(0.78,1.00) 1.00(0.78,1.00) 1.00(0.78,1.00) 1.00(0.78,1.00) 1.00(0.78,1.00)
Log_10(R0)(95%CI)
Sub-region Site Base CCSM4 MPI-ESM-MR CanESM MIROC5i M3 -0.3(-0.7,-0.0) -2.1(-2.4,-1.7) -1.5(-1.8,-1.1) -2.4(-2.7,-2.0) -0.2(-0.4,-0.0)i S1 0.7(0.2,1.1) -0.5(-0.9,-0.0) -1.5(-2.0,-1.0) -2.8(-3.0,-2.5) -0.2(-0.6,0.1)i M4 1.0(0.7,1.4) -0.0(-0.5,0.5) -0.3(-0.7,0.1) -2.4(-2.7,-2.1) 0.8(0.5,1.0)ii M1 -1.9(-2.4,-1.4) -2.8(-3.0,-2.6) -3.0(-3.0,-3.0) -3.0(-3.0,-3.0) -2.5(-2.8,-2.2)ii M2 -2.2(-2.7,-1.7) -2.7(-3.0,-2.4) -2.8(-3.0,-2.6) -2.9(-3.1,-2.8) -1.9(-2.2,-1.6)ii N1 -0.7(-1.1,-0.4) -1.3(-1.7,-0.9) -2.2(-2.6,-1.7) -2.2(-2.6,-1.7) -0.8(-1.0,-0.6)iii N2 0.0(-0.3,0.3) 0.2(-0.2,0.6) -0.8(-1.1,-0.5) -0.1(-0.3,0.1) 1.0(0.8,1.3)iii N3 1.0(0.7,1.3) 0.9(0.6,1.1) -0.2(-0.5,0.0) -0.1(-0.4,0.1) 1.2(1.1,1.4)iv M5 1.6(1.5,1.8) 1.4(1.2,1.6) 1.2(0.9,1.4) 1.2(0.9,1.5) 1.5(1.3,1.6)iv M6 2.0(1.9,2.2) 2.1(1.9,2.2) 1.9(1.8,2.0) 1.5(1.4,1.6) 2.3(2.2,2.4)iv NA1 1.6(1.3,1.8) 1.7(1.6,1.9) 1.4(1.1,1.7) 1.7(1.5,1.9) 2.0(1.9,2.1)iv M7 1.9(1.8,2.0) 2.1(2.0,2.3) 1.9(1.8,2.1) 1.6(1.5,1.6) 2.4(2.2,2.5)
PeakPrevalenceinchildrenaged2-10(95%CI)
Sub-region Site Base CCSM4 MPI-ESM-MR CanESM MIROC5i M3 2%(1,3) 3%(2,4) 2%(1,3) 3%(1,5) 3%(1,4)i S1 11%(2,20) 2%(1,2) 2%(1,2) 2%(2,3) 2%(1,2)i M4 46%(34,58) 9%(5,14) 4%(2,6) 9%(5,14) 17%(7,28)ii M1 1%(1,1) 1%(1,1) 1%(1,1) 2%(1,2) 1%(1,2)ii M2 2%(1,3) 2%(1,3) 2%(1,3) 3%(2,5) 2%(1,4)ii N1 2%(1,3) 2%(1,3) 2%(1,2) 2%(1,4) 2%(0,4)iii N2 2%(1,4) 4%(1,6) 2%(1,4) 4%(0,8) 19%(8,29)iii N3 23%(11,35) 13%(10,16) 4%(2,6) 4%(0,8) 26%(19,33)iv M5 42%(26,57) 43%(26,60) 30%(13,47) 27%(8,46) 29%(18,40)iv M6 66%(57,75) 67%(59,76) 64%(55,74) 33%(18,48) 69%(61,78)iv NA1 48%(29,67) 66%(52,80) 54%(38,70) 55%(38,71) 66%(51,80)iv M7 65%(55,74) 67%(57,78) 66%(57,76) 35%(19,51) 69%(59,79)
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Supplementary Table 2: Coefficient of determination (R2) values for annual rainfall, TJAS and indices of malaria transmission
TJAS log10(R0) log10(EIR) Pr2-10 ImmAnnualrainfall 0.51 0.72 0.81 0.62 0.68
TJAS 0.67 0.64 0.52 0.42log10(R0) 0.87 0.51 0.53log10(EIR) 0.7 0.81Pr2-10 0.65
Allpairsofvariablesarecorrelatedwithsignificancelevelsp<<0.0001
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Supplementary Table 3: Coefficients and statistics of regression model.
Regressionmodelstaketheformoff(TJAS,rain)=a+b*TJAS+c*rain/1000
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Supplementary Table 4: Summary of data sources
Datasource Spatialresolution
Temporalresolution
Reference
BaselineClimatology
temperature CRUTS3.21 0.5x0.5degree
1month1901-2012
35
rainfall CRUTS3.21 0.5x0.5degree
1month1901-2012
35
MeteorologicalInputsforHYDREMATSSimulation
precipitation CMORPHversion1.0 ~8km 30min1998-present
1
temperature ERA-Interim .75x.75degree
3hour1979-present
8
windspeed ERA-Interim .75x.75degree
3hour1979-present
8
winddirection ERA-Interim .75x.75degree
3hour1979-present
8
surfaceradiation ERA-Interim .75x.75degree
3hour1979-present
8
Othermodelinputs
soiltype HarmonizedWorldSoilDatabase
~1km Static 10
vegetation UniversityofMarylandLandcover
1km Static 9
topography ComputedfromEnvisatsyntheticapertureradarandgroundsurvey
10m Static36
householdlocations Quickbirdimage 0.6m Static 26
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Supplementary Table 5: Performance of CMIP5 Climate Models
ModelName RainfallScore TemperatureScore Total
Zone1 Zone2 Zone3 Zone1 Zone2 Zone3
BNU-ESM 1 1 1 1 1 1 6
MIROC5 1 1 1 1 1 5
MPI-ESM-MR 1 1 1 1 4
CANESM2 1 1 1 3
CCSM4 1 1 1 3
FGOALS-g2 -1 1 1 1 2
CESM1-CAM5 1 1 2
MIROC-ESM-CHEM 1 1
FIO-ESM 1 1
BCC-CSM1-1 1 1
CNRM-CM5 -1 1 1 1
CSIRO-Mk3-6-0 -1 -1 1 1 1 1
CMCC-CM 0
GFDL-CM3 0
GISS-E2-H -1 -1
HadGEM2-AO -1 -1
ACCESS -1 -1 -2
MRI-CGCM3 -1 -1 -1 -3
EC-EARTH -1 1 -1 -1 -1 -3
IPSL-CM5A-MR -1 -1 -1 -3
GFDL-ESM2M -1 -1 -1 -3
inmcm4 1 -1 -1 -1 -1 -3
HadGEM2-CC -1 -1 -1 -1 -1 -5
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