RESEARCHARTICLE Towards a DNA Barcode Reference Database for Spiders and Harvestmen of Germany JonasJ.Astrin1*,HubertHöfer2*,JörgSpelda3*,JoachimHolstein4*,SteffenBayer2, LarsHendrich3,BernhardA.Huber1,Karl-HinrichKielhorn5,Hans-JoachimKrammer1, MartinLemke6,JuanCarlosMonje4,JérômeMorinière3,BjörnRulik1,MaltePetersen1, HannahJanssen1,ChristophMuster7 1 ZFMK:ZoologischesForschungsmuseumAlexanderKoenig,Bonn,Germany,2 SMNK:Staatliches MuseumfürNaturkundeKarlsruhe,Karlsruhe,Germany,3 ZSM:ZoologischeStaatssammlungMünchen, München,Germany,4 SMNS:StaatlichesMuseumfürNaturkundeStuttgart,Stuttgart,Germany,5 Karl- a11111 HinrichKielhorn,Berlin,Germany,6 MartinLemke,Lübeck,Germany,7 ZoologischesInstitutundMuseum, UniversitätGreifswald,Greifswald,Germany *[email protected](JJA);[email protected](HH);[email protected](JS);joachim. [email protected](JH) Abstract OPENACCESS Citation:AstrinJJ,HöferH,SpeldaJ,HolsteinJ, AspartoftheGermanBarcodeofLifecampaign,over3500arachnidspecimenshavebeen BayerS,HendrichL,etal.(2016)TowardsaDNA collectedandanalyzed:ca.3300Araneaeand200Opiliones,belongingtoalmost600spe- BarcodeReferenceDatabaseforSpidersand cies(median:4individuals/species).Thiscoversabout60%ofthespiderfaunaandmore HarvestmenofGermany.PLoSONE11(9): e0162624.doi:10.1371/journal.pone.0162624 than70%oftheharvestmenfaunarecordedforGermany.Theoverwhelmingmajorityof speciescouldbereadilyidentifiedthroughDNAbarcoding:mediandistancesbetweenclos- Editor:MatjaKuntner,ScientificResearchCentreof theSlovenianAcademyofSciencesandArt, estspecieslayaround9%inspidersand13%inharvestmen,whilein95%ofthecases, SLOVENIA intraspecificdistanceswerebelow2.5%and8%respectively,withintraspecificmediansat Received:June3,2016 0.3%and0.2%.However, almost20spiderspecies,mostnotablyinthefamilyLycosidae, couldnotbeseparatedthroughDNAbarcoding(althoughmanyofthempresentdiscrete Accepted:August25,2016 morphologicaldifferences).Conspicuouslyhighinterspecificdistanceswerefoundineven Published:September28,2016 morecases,hintingatcrypticspeciesinsomeinstances.Anewprogramispresented:DiS- Copyright:©2016Astrinetal.Thisisanopen tatscalculatesthestatisticsneededtomeetDNAbarcodereleasecriteria.Furthermore, accessarticledistributedunderthetermsofthe newgenericCOIprimersusefulforawiderangeoftaxa(alsootherthanarachnids)are CreativeCommonsAttributionLicense,whichpermits unrestricteduse,distribution,andreproductioninany introduced. medium,providedtheoriginalauthorandsourceare credited. DataAvailabilityStatement:Allrelevantdataare withinthepaperanditsSupportingInformationfiles. Sequencesareappendedasalignment,theirtrace Introduction filesareavailablefromBOLD(http://www. boldsystems.org/).TheDiStatsscriptisavailable Long-termmonitoringofbiodiversityisoneofthemostimportantchallengesinconservation throughGitHub(https://github.com/mptrsen/distats) biology.To evaluatetheconservationstatusandanthropogenicimpactofhabitats,sufficient andthroughtheZFMKhomepage(www.zfmk.de/en/ research/research-centres-and-groups/distats). knowledgeonspeciescompositionofnaturalenvironmentsisneededonaregionallevel.For manyifnotmostinvertebratetaxa,wearestillfarfromachievingthisgoal.Onepromising Funding:TheGBOLprojectisfinancedbythe approachtomeetthischallengeisDNAbarcoding[1],atechniquethatusestheeasytohomol- GermanFederalMinistryofEducationandResearch (BMBF#01LI1101).Partofthesequencescontributed ogize,well-quantifiable,discretetaxonomiccharacterscontainedinDNAsequencedatafor byZSMresultedfromfundingbytheBavarianState standardized,rapid,andrelativelycheapspeciesidentification.DNAbarcodingdependson PLOSONE|DOI:10.1371/journal.pone.0162624 September28,2016 1/24 DNABarcodingofSpidersandHarvestmeninGermany MinistryofEducationandCulture,Scienceandthe lowlevelsofintraspecificvariationcoupledwithmarkedgeneticdifferentiationbetweenspe- Arts(BarcodingFaunaBavarica,BFB).The cies(the'barcodinggap',investigatedinspidersin[2–4]). sequencingworkofZSMwassupported,inpart,by Withmorethan45,800describedspecies[5],spidersareamongthemostdiverseanimal fundingfromtheGovernmentofCanadatoGenome orders[6].Theyareabundantinallterrestrialhabitats.Asubiquitouspredators,theyoccupya CanadathroughtheOntarioGenomicsInstitute,while theOntarioMinistryofResearchandInnovationand keypositioninfoodwebs.Manyspeciesshowpreferencesforspecifichabitatstructuresor NSERCsupporteddevelopmentoftheBOLD environmentalfactors,e.g.temperature,humidity,shading[7],whichturnsthemintopotential informaticsplatform.Thefundershadnoroleinstudy indicators[8].Easytoobserveanddocument,spidersareseenasamodelgroupforecological design,datacollectionandanalysis,decisionto studies[9,10]. publish,orpreparationofthemanuscript. ThespiderfaunaofGermany,comprisingapproximately1000species[11],iswellknown, CompetingInterests:Theauthorshavedeclared andchecklistsandredlistsofendangeredspecieshavebeenpublishedforGermanyandmost thatnocompetinginterestsexist. ofitsfederalstates(see[11]andreferencestherein).The'ArachnologischeGesellschafte.V.' (www.arages.de)offersregularlyupdatedoccurrencemaps,basedonasteadilygrowingdata- base.Therefore,spidersareregularlyusedinhabitatassessments,biodiversityinventories,and ecologicalstudies(e.g.[12–18]).Spidersareparticularlypromisingasindicatorsofsustainable forestmanagement[19],habitatstructure[20],successionalstages[21,22],orconservation value[23,24].Therehavebeenseveralattemptstoclassifyspidersaccordingtotheirhabitator nichepreferencesinGermanyorCentralEurope[7,25–30]andtousethesedatatoclassify habitatsorassesshabitatqualitybyidentifyingtheproportionofrare,endangered,stenotopic, orcharacterspecies(e.g.[18,31,32]).IdentificationofGermanspidersisfacilitatedbythe onlinekeysforspidersofEuropeatwww.araneae.unibe.ch[33].However,morphologicaliden- tificationtospecieslevelrequiresadultspecimensinmostinstances.About80–200spiderspe- ciescanoccurinanear-naturalhabitatinGermany,ofwhichonlyasmallfractioncanbe directlyrecordedandidentifiedinthefield(pers.obs.,H.Höfer,C.Muster).Foranecolog- icallymeaningfulassessmentoraclosetocompleteinventory,muchmoretimeneedstobe investedtocapture,process(oftenmeaningdissectionofsexualorgans)andidentifythe (adult)spiders,requiringconsiderableexpertise.Regularly,severalspecimensremainthathave tobecheckedbythefewavailabletaxonomicspecialistswithsufficientknowledgeonmorpho- logicalvariabilityintherespectivespeciesandwithaccesstoreferencecollections. Withsome6500speciesworldwide,harvestmen(Opiliones)constitutethethird-largest orderofarachnids[34].Currently,52specieshavebeenrecordedfromGermany[35].The omnivorousharvestmenconstitutearegularcomponentofterrestrialfaunas,withhighestden- sitiesindampandshadedhabitats[36].Theiruseinappliedandecologicalstudiesisexplained bytheexistenceofbothstenotopicspecieswithstrictmicrohabitatrequirements(andoften limitedgeographicranges)andinvasivespeciesthatexhibitimmensecolonizationpotential [37,38].DeterminationofmostGermantaxaisreliablyachievableusingtheworkof[39]. However,recentstudieshaverevealedhighlevelsofcrypticdiversityinCentralEurope[40– 42],suggestingapromisingperspectiveforDNAbarcodinginthistaxon. TheuseofmitochondrialCOIbarcodes[43]fromanextensivereferencedatabaseofspider andharvestmenspecieswillaidnon-specialistsinthedeterminationofthesegroups.Species thathavehithertobeenproblematicorevenimpossibletoidentifymorphologically–eitherin generalorforaparticularsex–maybereliablydiscriminated.EventhoughnotfrequentinGer- many, therearestillmanyspiderspeciesinwhichoneofthe(dimorphic)sexesisstill unknown,andbarcodingcanprovidethelinkbetweensexes(demonstratede.g.in[44]).More- over,disputedinstancesofsynonymymayberesolved[45].Notleast,aconsiderableadvantage ofbarcodingisthepossibilitytoidentifyjuvenilespecimens[3,46–49].Thiswillnotonlymake inventoriesmorecomplete,butwillalsoallowspecies-levelinclusionofjuvenilesintoecologi- calanalyses.Tapping intothisrichmaterialresourcewillallowstudyingmoreecologicalques- tionswithoutthenecessityforexhaustiveandexpensivesampling.Afuturebroadapplication ofroutineDNAbarcodinginspidersisfacilitatedthroughmass-trapping,sincesomeofthe PLOSONE|DOI:10.1371/journal.pone.0162624 September28,2016 2/24 DNABarcodingofSpidersandHarvestmeninGermany samplingsolutionsemployedintrapspreserveDNAwellenoughforbarcoding[50,51].The methodfurtherholdsthepotentialtorevealcrypticspeciesortoidentifycaseswheremorpho- logicalplasticitymayhavebeenover-interpreted.Barcodingmaythusactasacatalystfor alphataxonomy[52].Whileintrogressionevents[53],retentionofancestralpolymorphisms [49],nuclearmitochondrialpseudo-genes[54]orendosymbionts(Wolbachia bacteriaetc.) [55,56]allposepotentialproblemstoDNAbarcodingapproaches,agrowingnumberofstud- iesshowthegeneralfeasibilityofDNAbarcodingforarachnids[2–4,46,47,57–66]. TheGermanBarcodeofLife(GBOL)campaignisimplementedbyanationalnetworkofca. 20biodiversityresearchinstitutionsandmorethan200taxonspecialists[67].Itpursuesthe goaltoestablishaDNAbarcodelibraryofasmanyanimal,fungalandplantspeciesaspossible thatoccurinGermany.Theprojectaimsatcollecting,ifpossible,tenspecimensperspecies, fromlocationsasdistinctaspossiblethroughoutthecountryinordertocapturegeneticvari- ability.Somespecieswithwiderrangesmayalsoincludespecimenscollectedinneighboring countries. NaturalhistorycollectionsconstitutethecoreinfrastructureofGBOL,takingintoaccount thatbarcodingprojectsproduceavaluablelegacyofvouchers(morphologicalspecimensand molecularsamplesalike)whichbecomerelevantinsubsequentstudiesduetothehighquality oftheunderlyingtaxonomicassignmentsandgranularityofthemetadata.Thesevouchers formthephysicalfoundationthatfuturemonitoringprojectswillbebasedon,warrantingcon- tinuoustestability,validation,andcoherentexpansionofthebarcodingreferencedatabase– ideallyforcenturiestocome. WithintheGBOLconsortium,arachnidshavereceivedwideattention,asnolessthanfour GBOLinstitutesandtheirrespectiveexternalarachnologistpartnerscollaborateintensivelyon compilinganationalmolecularinventoryofspidersandharvestmen:StaatlichesMuseumfür NaturkundeKarlsruhe(SMNK),StaatlichesMuseumfürNaturkundeStuttgart(SMNS),Zool- ogischesForschungsmuseumAlexanderKoenig(ZFMK),andZoologischeStaatssammlung München(ZSM).AcariarebeinginvestigatedinanotherGBOLsubproject(bySenckenberg MuseumfürNaturkundeGörlitz,SMNG). Forspiders,country-focused,taxonomicallybroadbarcodingdatasetshavesofarbeenpub- lishedforCanada[61](1018speciescovered),forSloveniaandforSwitzerland[66](together 298species)and,inapilotproject,fortheNetherlands[68](31species)(foralistofongoing Europeanprojects,seehttp://www.araneae.unibe.ch/barcoding/content/15/Barcoding-of- European-spiders).Thepresentstudycontributesthefirstdatasetofaspiderbarcodingcam- paignforGermanyandthefirstdatasetworldwideofthiskindforharvestmen. MaterialsandMethods Sampling Forthisstudy,3537arachnidspecimens,3339Araneaeand198Opiliones,weresampledfrom Germany(91%ofthematerial)andneighboringcountries.WithinGermany,24%ofthespeci- menswerecollectedinBaden-Württembergand13%inSchleswig-Holstein.MostotherGer- manstateswererepresentedby6–10%oftheGermanspecimenseach.Thuringia(0.1%), Hesse(1%)andRhineland-Palatinate(2%)werelesswellrepresented,aswerethecity-states andthecomparativelysmallSaarland(1%).Fig1illustratesthesamplingpattern. SMNKandexternalpartnersareresponsibleforandcontributed14%ofthespecimens, SMNSandpartners10%,ZFMKandpartners56%,ZSMandpartners20%. To date598morphologicalarachnidspecies(561spp.inspidersvs.37inharvestmen)in 269genera(246vs.23)and50families(44vs.6)couldbeintegrated.Settingthisintorelation PLOSONE|DOI:10.1371/journal.pone.0162624 September28,2016 3/24 DNABarcodingofSpidersandHarvestmeninGermany Fig1.Geographicsamplingofarachnidspecimensunderlyingthepresentstudy.ImageproducedusingGPSVisualizer (www.gpsvisualizer.com). doi:10.1371/journal.pone.0162624.g001 PLOSONE|DOI:10.1371/journal.pone.0162624 September28,2016 4/24 DNABarcodingofSpidersandHarvestmeninGermany Fig2.Numberofspeciessampledperfamily(excludingfamiliesrepresentedonlyby1or2speciesinthisstudy).Numbersabovebarsare percentagesshowingspeciescoverageforGermany,asderivedfromthechecklistsmentionedinthetext.Familynamesprefixedwith"O."belongto Opiliones,allothersarespiderfamilies. doi:10.1371/journal.pone.0162624.g002 withtheGermanchecklists[11,35],speciescoverageis57%forspidersand71%forharvest- men.SpeciesnumbersareplottedforthemorefrequentfamiliesinFig2. Thespeciesinthedatasetwererepresentedby6individualsonaverage(median:4).Almost 19%,i.e.112species,were'singletons'.With48specimens,Pardosalugubriswasthespecies withmostindividuals;allotherspecieswererepresentedby30orfewerindividuals(seeFig3). Mostindividuals(98%)werecollectedspecificallyforGBOLbetweentheyears2011and 2015.Theoldestspecimenprocessedinthisstudywascollectedin2003. Collectingwasmostlydonebyhand,andmostspecimenswerekilledandpreserveddirectly in96%or100%ethanol.7%ofthespecimenswereinitiallypreservedin70%water-dilutedeth- anoland8%werecollectedinpropyleneglycol.Thelatterwasusedascapturefluidinpitfall traps;soonafteridentification,tissueforDNAextractionwastransferredtoabsoluteethanol. Allmaterialusedinthisstudyispropertyofthefederalstatesoftheinvolvedinstitutions. Materialacquiredbytheseinstitutionsisonlyacceptedafteracheckthatitwascollectedin compliancewithnationalandinternationallaws,regulationsandconventionsandthatthe materialisfreefromthirdpartyrights.Furthermore,inordertobecomecertifiedasaGBOL collector,itisrequiredtoaccepttheproject'sgeneraltermsandconditions,whichdemand abidingbytheregulationsoftheConventiononBiologicalDiversityandnationallegislations. Fieldworkpermitswereissuedbythefollowingauthorities:BayerischesStaatsministeriumfür PLOSONE|DOI:10.1371/journal.pone.0162624 September28,2016 5/24 DNABarcodingofSpidersandHarvestmeninGermany Fig3.Numberofspecimenssampledperspecies.19%ofthespecieswere'singletons',whilethemedianrepresentationlayat4individualsper species. doi:10.1371/journal.pone.0162624.g003 UmweltundGesundheit,München;RegierungspräsidiumStuttgart;Regierungspräsidium Karlsruhe;Struktur-undGenehmigungsdirektionKoblenz;KreisverwaltungRhein-Sieg-Kreis, AmtfürNatur-undLandschaftsschutz;AmtfürUmwelt,Verbraucherschutz undLokale Agenda,UntereLandschaftsbehörde,Bonn;NationalparkamtMüritz,Hohenzieritz;Biosphär- enreservatsverwaltungNiedersächsischeElbtalaue,Hitzacker;NationalparkforstamtEifel, Schleiden-Gemünd;AmtfürdasBiosphärenreservatSüdost-Rügen,Putbus;Landesamtfür Umwelt,NaturschutzundGeologieMecklenburg-Vorpommern,Güstrow;Landesamtfür Landwirtschaft,UmweltundländlicheRäumeSchleswig-Holstein,Flintbek;LandratKreis HerzogtumLauenburg;LandratKreisRendsburg-Eckernförde,FachdiensteuntereNat- urschutzbehörde.Thepermitscoverstateforests,publiclandandprotectedareasaswellasthe fivespeciesofArachnidaprotectedinGermany:Arctosacinerea,Dolomedesfimbriatus,Dolo- medesplantarius,EresuscinnabarinusandPhilaeuschrysops. Altogether,over100collectorscontributedmaterial.Fielddataforallanalyzedspecimens canbeaccessedinS1Table.Juvenilespecimensanalyzedbelongtotaxathatareeasilyidentifi- ablealsoinjuvenilestage(e.g.basedoncoloration)orforwhichproblematic('look-alike')con- genersdonotoccurinthestudyarea.Juvenilesthatclusteredconspicuouslyinthetreewere removedfromthedataset. Allmorphologicalspecimenvouchersandalsomolecularvouchers(DNAandoftentissue) aredepositedatandareavailablefromthefollowingfourGermanpubliccollections(perma- nentrepositories):StaatlichesMuseumfürNaturkundeKarlsruhe(SMNK),Staatliches MuseumfürNaturkundeStuttgart(SMNS),ZoologischesForschungsmuseumAlexanderKoe- nig(ZFMK),Bonn,ZoologischeStaatssammlungMünchen(ZSM).Allvouchernumbersare giveninS1Table.ThevoucherIDsinS1Table aswellasthenamesinthetreesincludethe institutionalcode,sothattheassociationofagivensampletooneoftheGBOLpartnerinsti- tutescanbeeasilyestablished. SequencedataareavailableonBOLD[69]viaDOIdx.doi.org/10.5883/DS-GBOLARA,and onGenBank.Specimendatawillalsobeaccessible,alongsidespecimenimages,throughthe GBOLportal(www.bolgermany.de). PLOSONE|DOI:10.1371/journal.pone.0162624 September28,2016 6/24 DNABarcodingofSpidersandHarvestmeninGermany Molecularmethods Analyseswereperformedmostlyinthreeseparatelaboratories:ZFMK,SMNS,andCanadian CentreforDNABarcoding(CCDB)inGuelph.SMNSandZFMKusedtheirownfacilities(up tothepointofsequencing),SMNKsampleswereprocessedatbothSMNSandZFMK,ZSM samplesatCCDB. Total genomicDNAwasusuallyisolatedfromlegs.Inverysmallspecimens(especially manyLinyphiidae)atZFMKandSMNS,DNAwasextractednon-destructivelyfromwhole specimenswhichwererecoveredafterlysis(cf.[70]). AtZSM,singlelegswereremovedfromeachspecimenandsentin96welllysisplatesto CCDBforstandardizedDNAextraction,PCRamplificationandbidirectionalSangersequenc- ing.CCDBlabprotocolsareavailableunderwww.ccdb.ca/resources.php. AtZFMKandSMNS,silica-basedmethodswereemployedtoextractDNA.SMNSfollowed theprotocolby[71]withPallAcroPrepTM96filterplates(PallCorporation,PortWashington, NY, USA),whileaQiagen(Hilden,Germany)BioSprint96magneticbeadextractorandcorre- spondingkitswereusedatZFMK. Polymerasechainreactionforthe5'partofthemitochondrialcytochromecoxidasesubunit 1(COI)genewascarriedout,atZFMK,intotalreactionmixesof20μl,including2μlofundi- lutedDNAtemplate,0.8μlofeachprimer(10pmol/μl),andstandardamountsofthereagents providedwiththe'MultiplexPCR'kitfromQiagen(Hilden,Germany).AtSMNS,PCRreac- tionsof25μlvolumecontained4μlDNA,5unitsofTaq KAPA extrapolymerase(KAPA- BIOYSYTEMS,Boston,USA),10μlof5xKAPA Taq extrabuffer,3μlofMgCl (25mM;both 2 solutionsprovidedbythemanufacturer),1μlofeachprimer(10pmol/μl),and1μlof10mM dNTPmix(Bioline,Luckenwalde,Germany). ThePCRprimersused(alsoforsequencing)aregiveninTable 1. Thermalcyclingwasperformed,atZFMK,onAppliedBiosystems2720ThermalCyclers (LifeTechnologies,Carlsbad,CA,USA),usingaPCRprogramwithtwocyclesets,asa Table1. Listofprimersusedforamplificationandsequencingofthe5'partofthemitochondrialCOIgene. Primername Sequence Publication Usedat LCO1490 5'-GGTCAACAAATCATAAAGATATTGG Folmeretal.1994 SMNS,CCDBforZSM,ZFMK HCO2198 5'-TAAACTTCAGGGTGACCAAAAAATCA Folmeretal.1994 SMNS,CCDBforZSM,ZFMK LepF1 5'-ATTCAACCAATCATAAAGATATTGG Hebertetal.2004 CCDBforZSM LepR1 5'-TAAACTTCTGGATGTCCAAAAAATCA Hebertetal.2004 CCDBforZSM C_LepFolF cocktailofLepF1andLCO1490 www.boldystem.org/index.php/Public_Primer_PrimerSearch CCDBforZSM C_LepFolR cocktailofLepR1andHCO2198 www.boldystem.org/index.php/Public_Primer_PrimerSearch CCDBforZSM LCO1490-JJ 5'-CHACWAAYCATAAAGATATYGG Astrin&Stüben2008 ZFMK HCO2198-JJ 5'-AWACTTCVGGRTGVCCAAARAATCA Astrin&Stüben2008 ZFMK LCO1490-JJ2 5'-CHACWAAYCAYAARGAYATYGG new ZFMK HCO2198-JJ2 5'-ANACTTCNGGRTGNCCAAARAATCA new ZFMK LCO1490-JJ4a 5'-CNACNAAYCAYARRGAYATYGG new ZFMK HCO2198-JJ4a 5'-AIACYTCNGGRTGICCAAARAATC new ZFMK LCO1490-JJ4 5'-CIACIAAYCAYAARGAYATYGG new ZFMK HCO2198-JJ4 5'-ANACTTCNGGRTGNCCAAARAATC new ZFMK Species—alsomanyothersthanarachnids—withstronglymodified bindingsitescouldusuallybesuccessfullyamplifie datZFMKwithasetofnewly (manually)designed,highlydegenerateprimers(mostoftenusingcombinationLCO1490-JJ2&HCO2198-JJ2).ThecombinationLCO1490-JJand HCO2198-JJconstitutesthestandardsetofprimersusedatZFMK.ThestandardsetofprimersusedatCCDBforZSMwasthecombinationC_LepFolF andC_LepFolR,acocktailconsistingoftheprimerslistedabove. doi:10.1371/journal.pone.0162624.t001 PLOSONE|DOI:10.1371/journal.pone.0162624 September28,2016 7/24 DNABarcodingofSpidersandHarvestmeninGermany combinationofa'touchdown'anda'step-up'routine:firstcycleset(15repeats):35sdenatur- ationat94°C,90sannealingat55°C(−1°Cpercycle)and90sextensionat72°C.Secondcycle set(25repeats):35sdenaturationat94°C,90sannealingat45°C,and90sextensionat72°C. AtSMNS,PCRamplificationwascarriedoutinaLabcyclerbySensoQuest(Göttingen,Ger- many).PCRconditionswere:35cyclesof60sdenaturationat93°C,90sannealingat50°Cand 60sextensionat72°C. PCRproductsweresubsequentlysentforbidirectionalSangersequencingtovariouscom- panies:ZFMKtoBGI(HongKong,China)andMacrogen(Amsterdam,Netherlands),SMNS toLGCGenomics(Berlin,Germany)in2013andfrom2014ontoGATCBiotech(Konstanz, Germany). DNAsequencealignmentwasperformedusingparallelizedMAFFTver.7.123[72].PAUP(cid:3) ver.4.0b10[73]wasusedforp-distancetransformationsandforevaluatingbasecomposition andinformationcontent.Statisticalparsimonynetworks[74]werecalculatedwiththeTCS algorithm[75]inPopART(http://popart.otago.ac.nz).Statisticalevaluationofthedatawas performedusingSPSS,R(boxplots),SpeciesIdentifierver.1.7.7–3[76](extractionof'splits' and'lumps'),andthePerlscriptDiStats(intraspecificdistances,individualizeddataonclosest speciespairsandonmostdistantcongeners).DiStatshasbeendevelopedforthisstudyandis available,includingdocumentation,underGitHub(https://github.com/mptrsen/distats)and throughtheZFMKhomepage(www.zfmk.de/en/research/research-centres-and-groups/ distats).ThescriptusesFASTA asinputformat,calculatesp-distancesorK2Pdistancesand canbeparallelizedinordertoprocesslargedatasets.Itcanproducetwooutputfiles:atable withstatisticsforeachspeciesandoptionallyalsothematrixofallpairwisedistancesinthe dataset.Foranalignmentcontaining1000COIbarcodesequences,theanalysiswilltake around6minuteswhenusingasinglethread(ona3.4GHzprocessor).DiStatshasanalgorith- miccomplexity(O)ofapproximatelyO(n2),whichmeansthatruntimeincreasesexponen- tiallywiththenumberofinputsequences(n).UsingmultipleCPUthreadsreducestherun timebyafactorof1/c,wherecisthenumberofthreads. PAUP wasalsousedforreconstructionofapheneticneighbor-joining(NJ;[77])treeasa quickmolecularidentificationcheck.PhylogeneticreconstructionsusingMaximumLikelihood (ML;[78])wereperformedwithRAxMLver.7.3.0[79].EvolutionarymodelselectionfortheML analysiswasimplemented,usinghierarchicallikelihoodratiotesting,inModelGeneratorver. 0.85[80]andindicatedGTR+I+Γasthebest-fittingmodel[81].TheCOIdatasetwasparti- tionedtotreat3rdcodonpositionsseparatelyfrom1stand2ndpositions.Theanalysiswasrun for1milliongenerationsandincluded1000bootstrapreplicates.FortreerootingpurposesinNJ andMLanalyses,wechoseamitesequencefromBOLDasoutgroup(seeS1Alignment). Results AverageCOIsequencelengthforthe3537sequenceswas650bp.To accommodatemany slightlyshortersequences,whileavoidinggeneticdistanceartifacts,alignmentlengthwassetto 653bp.Sequencesshorterthan500bpwereexcludedfromtheanalysis.Theshortestincluded sequencewascomposedof509residues. Thedatasetcomprised2099distincthaplotypes,meaningthat1438sequenceswerenon- unique. Amongnucleotides,therewasacompositionalbiastowardsAT: 67.5%,whichiscloseto levelspreviouslyreportedforspiders(e.g.[4,82,83]).Indetail,overallbasecompositionwas:A 25.3,C13.3,G19.2,T42.2%. Altogether,5,572,791pairwisedistanceswerecomputedforspiders;ofthese,17,867were intraspecificdistances.ForOpiliones,therewere19,503pairwisedistancesofwhich896were PLOSONE|DOI:10.1371/journal.pone.0162624 September28,2016 8/24 DNABarcodingofSpidersandHarvestmeninGermany Table2. Estimatorsusedtocharacterizegeneticdistancestructureinthedataset. [%] intraspecific interspecific median mean range 95thperc. median mean range 5thperc. Araneae 0.3 0.7 0.0–10.1 2.5 17.5 17.4 0*-28.2 13.6 Opiliones 0.2 1.3 0.0–8.9 8.1 19.3 19.4 7.0–30.1 13.6 Aran.K2P 0.3 0.7 0.0–11 2.6 20.0 20.0 0.0–35.6 15.0 Opil.K2P 0.2 1.3 0.0–9.5 8.7 22.6 22.7 7.5–38.6 15.1 Theuppertworowsindicateuncorrecteddistancesforspidersandharvestmen,respectively,whilethethirdandfourthrowsgiveK2Pdistances(asrequired forabarcodedatarelease).Medianandmeandistancesaregivenforbothintraspecific andinterspecific distances,alongwiththerangebetweenthe smallestandlargestobservationintherespectivedatacategory.*:Therewerecasesofsharedhaplotypesamongspecies,seetext. doi:10.1371/journal.pone.0162624.t002 distancesbetweenconspecificspecimens.Table2givesanoverviewofintra-andinterspecificdis- tances,separatedbyorder.Table3summarizesdistancesforallclosestspeciespairsandforthe mostdistantcongenericpairs;S2andS3Tablesillustratetheseinmoredetail,givingindividual statisticsbytaxon.S2Table(spiders)andS3Table(harvestmen)furthermoreindicateintraspecific distancerangesandcentraltendenciesforallanalyzedspecies.S4Tableindividuallyliststhehigh- estintraspecificdistancesinthedataset,whileS5Tablegivesthelowestinterspecificdistances. Therangecoveredbyintraspecific(p-)distanceswassimilarforspiders(0–10%)andhar- vestmen(0–9%),withanarithmeticmeanof0.7%inspidersand1.3%inharvestmen.The influenceofhighoutlierswasstrongerinthecomparativelysmallharvestmandataset(median at0.2%vs.meanat1.3%),causedmostlybythedeepsplitswithinMitopusmorio(Fabricius, 1779)andPhalangiumopilioLinnaeus,1758(bothdiscussedbelow),butalsoinNemastoma lugubre(Müller,1776)(seeS4Table). Theinterspecificdistancerangevariedforthetwoarachnidorders:0.0–28%inspiders, 7–30%inharvestmen.Infourcases,haplotypesweresharedamongnominalspiderspecies (seeS5Table,alldiscussedbelow):EnoplognathalatimanaHippa&Oksala,1982/E.ovata (Clerck,1757);Pardosalugubris(Walckenaer, 1802)/P.saltansTöpfer-Hofmann, 2000;Tibel- lusmaritimus(Menge,1875)/T.oblongus(Walckenaer, 1802);Xysticusaudax(Schrank, 1803)/X.cristatus(Clerck,1757).Interspecificarithmeticmeanswere17%forspiders,19% forharvestmen. Table3. Statisticsforclosestspeciespairsandmostdistantcongenericpairs. [%] closestspeciespairs mostdistantcongenerpairs range median(ofalldist.forspeciespairs) range median(oflargestdistances) Araneae 0.0*-20.1(22.0) 9.2 1.8–20.2 11.8 Opiliones 7.0–21.8(22.8) 13.8 12.6–18.8 14.9 AraneaeK2P 0.0–21.0(28.6) 9.9 1.9–23.8 12.8 OpilionesK2P 7.5–24.0(29.0) 15.5 13.7–22.0 16.5 Theuppertworowsindicateuncorrecteddistancesforspidersandharvestmen,respectively,whilethethirdandfourthrowsgiveK2Pdistances(asrequired forabarcodedatarelease).Therangefortheclosestspeciespairsindicatestheminimumandmaximumamongallsmallestpairwisedistancesbetween closestspeciespairs.Ifaclosestspeciespairisrepresentedbyseveralindividuals,theremaybelargerdistancesaswell:themaximalclosestspecies distanceintherespectivedatasetisindicatedinparentheses.Whilefortheclosestspeciespairsnoclassific atorial(genus)backgroundinformationwas used,thelasttwocolumnsinthistableorientthemselvesatdistancesfromrepresentativeswithinthesamegenus(butdifferentspecies).Therangeforthe mostdistantcongenerpairsextractstheextremesamongthesemaximalpairwisedistancesbetweenfarthestcongenericspeciespairs.Informationonthe individualclosestspeciespairsandontherespectivemostdistantcongenericspeciespairsisgiveninS2TableforspidersandS3Tableforharvestmen. *Therewerecasesofsharedhaplotypesamongspecies,seetext. doi:10.1371/journal.pone.0162624.t003 PLOSONE|DOI:10.1371/journal.pone.0162624 September28,2016 9/24 DNABarcodingofSpidersandHarvestmeninGermany Fig4.Boxplotofp-distancesfortheorderAraneae.Sortedbydistancecategory:betweenspecimensofdifferentgenera(allogeneric),between specimensbelongingtodifferentspecies,buttothesamegenus(congeneric),andbetweenspecimensthatbelongtothesamespecies(intraspecific). Boxesindicateinterquartilerange(IQR:betweenupper[Q3]andlower[Q1]quartile).Blackbarsdesignatemedians,whiskersindicatevalueswithin 1.5×IQRbeneathQ1or1.5×aboveQ3.Circlesdepictoutliers(aboveorbelow1.5×IQR). doi:10.1371/journal.pone.0162624.g004 Meanintraspecificdistancesvariedconsiderablyamongfamilies.Forthebest-represented spiderfamilies,theselaybetween0.4%(Agelenidae,Lycosidae,Philodromidae)and1.0%(Tet- ragnathidae).Clubionidae,LinyphiidaeandTheridiidaehadmeanintraspecificdistancesof 0.6%,Gnaphosidae0.7%,Araneidae0.8%,SalticidaeandThomisidae0.9%. Table 2andtheboxplots(Figs4and5)indicatethatauniversalbarcodinggapisabsent fromthedataset.However,mostofthespeciesseparatewell;whenignoringthe5%most extremeoutliers(ahypotheticalscenarionotsurpassingtheusualsignificancethreshold),the barcodinggapforharvestmenwouldspan5.5%andforspiderseven11%(seeTable 2).The mediandistanceforclosestspeciespairswas9%inspidersand13%inharvestmen. ApheneticreconstructionusingNeighborJoining(NJ;S1Fig)andaphylogeneticrecon- structionusingMaximumLikelihood(ML;S2Fig)deliveredtreesinwhichthespeciesover- whelminglyformedmonophyleticclusters(butseediscussion–severalofthecaseswith conspicuousdistanceswerealsorecoveredasparaphyleticandpolyphyletic).MLbootstrap analysispredominantlyindicatedveryhighsupportforspecies-levelnodes,butdidusuallynot allowmuchinsightintodeepertreetopology. Discussion ManypreviousstudiesusingCOIhaveshownthatspeciesdifferentiationviaDNAbarcoding isgenerallyfeasibleandpromisinginarachnids(mostlyspiders:e.g.[2–4,46,47,57–66]–butsee PLOSONE|DOI:10.1371/journal.pone.0162624 September28,2016 10/24
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