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Residence and territorial characteristics of Libellulidae species in a neotropical assemblage (Anisoptera) PDF

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Odonatologica37(3):213-220 September1,2008 Residence andterritorial characteristics of Libellulidaespecies ina neotropicalassemblage (Anisoptera) D.C. Resende¹*and P.De Marco+Jr². 1 Laboratorio deEcologiaeSolos,CursodeCiencias Biologicas, Centro Universitario do LestedeMinas Gerais,R. BarbaraHeliodora,725 Bom Retiro, BR-35160-215,Ipatinga,MG, Brazil [email protected] 2Laboratorio deEcologiaTeorica eSintese,DepartamentodeBiologiaGeral, Universidade Federal deGoias,BR-74001-970,Goiania,Goias,Brazil [email protected] ReceivedFebruary25, 2007/Revised andAcceptedDecember30,2007 Duringterritorial behaviour,aggressive attacksamongheterospecificodon. 33 arecommonand maycauseaseparationofniches, based onthepreferredsites for territorial defence. Here,territorial behaviourand thecharacteristics ofterritories in <JdofErythrodiplaxmedia,Micrathyriacatenataand M.hesperisaredescribed and theirterritorial fidelity, capturingandmarkingof<3 3arediscussed. Inallspp. stud- ied,there wasacleardistinctionamongthe microhabitatsdefendedasterritories. In both Micrathyriaspp., 3 3 seemtodefendterritories with defined resources.InE. media,thedefended resourcesarelessevident.Its3 3arehighlyaggressiveandshow highterritorial fidelitybut,apparently,theylosethe territoryiftheystay awayfrom waterforatleast oneday. INTRODUCTION During territorialdefence, aggressive attacks amongheterospecific odonate malesare common(HASSAN, 1978; MAY, 1980)andcompetition and aggres- sive interactionscouldcausesomespecies tochange theirhabitatselection(MAY, 1980;RUSSELL etal., 1998). Theseaggressive interactions may cause asepa- rationofniches amongspecies. Thusthe co-occurring species, Ischnuraelegans (VanderL.),Coenagrion pulchellum (VanderL.), Enallagma cyathigerum(Charp.) andErythromma najas(Hans.), forexample, haveenough differentiationintheir oviposition sites(JOHANNSSON, 1978). Sympetrumflaveolum (L.)malesuse *Correspondingauthor 214 D.C. Resende& P.DeMarcoJr lowerperches than thoseof S.sanguineum (Mull.) butbothspecies perch lower whentheirneighbour is amaleoftheotherspecies (REHFELDT & HADRYS, 1988). Differences in territorial qualitybetween odonate species are littleevident. In somespecies, malesdefendedterritories selected by the femalebasedon the quantityofoviposition resourceavailable(TSUBAK1&ONO, 1986;ALCOCK, 1987a; ALCOCK, 1987b; KOENIG, 1991; MEEK & HERMAN, 1991;BAT- TIN, 1993),whereasinotherspecies, territorial defenceseemstobemorerelated to thechanceofmales detecting femalesarrivingatthepond(ALCOCK, 1987a, 1987b; VAN BUSKIRK, 1986; BATTIN, 1993; DE MARCO& RESENDE, 2004)andinthis case,thesizeoftheterritory candeterminereproductivesuccess of somespecies, sinceit increases thechanceofmalevisualizing females(VAN BUSKIRK, 1986).Theperches orsubstrates forthemaleperching inaterritory canalsobe diverse(PARR, 1983;OSBORN & SAMWAYS, 1996),andchange mainly as afunctionoftheiravailability. The objective ofthisstudy was to determinethe criteria forselection of ter- ritoriesby males of Erythrodiplax mediaBorror, Micrathyria catenata Calvert, and M. hesperis Ris, by observing theirterritorialbehaviour, territorialfidelity, andthe characteristicsoftherespective territories. METHODS STUDY AREA - The work wascarried out duringFebruary-April in the Centrode Estudos deFlorestasNaturaisof Universidade Federal deViposa,MinasGerais(20°45’S,42°5TW).There- gionalclimate isCwa (Kdppenclassification),moderatelyhumid sub-tropicalwith ahidric deficit between May andSeptember(GOLFARI, 1975).Theaverageannualrainfall is1450mm,relative air humidityca80%and thetemperature varyingfromamaximum of26,1°Ctoaminimum of 14,0°C (VALVERDE, 1958). Duetoalocal dam,Nympheacf.amplaandEleocharis areveryabundantinthecoastalregion.At the shoreline therearesticksand grassesthat areused asperchesbysomedragonflyspecies. BEHAVIOUR ANDTERRITORIALCHARACTERISTICS - Duringthe studyperiod,all activities relativetoterritorial defence,matingritual and ovipositionwererecorded. The emphasis wasondescriptionsofthebehaviour,courtshipritualbefore mating,maledefencebehaviourduring ovipositionand ontheovipositionsites. Tocharacterize theterritories defended by E. media, M. catenata and M. hesperis, wewalked aroundtheshoreline ofthepondandrecorded,foreach individual,thetypeand heightofitsperch, thedistancefromtheperchtothe shoreline,thevegetationsurroundingtheperchand thedistance betweenperches oftheconspecificterritorialmales. Todetermineinterspecificdifferencesintheter- ritorial characteristics,weperformedanalyses ofChi-squareforcategorical variables and analyses ofvariance (ParametricANOVAand Kruskal Wallis)forquantitativevariables. TERRITORIALFIDELITY— Forthesakeoftheenquireintotheuseoftheterritoriesbymales ofthethreespecies, 12adjacentsectionsoffivemeterslengthweremarked in thelittoralzoneofthe pond.Maleswerecapturedand markedonthewingswith non-toxicpaint.Thedateofcaptureand thesectionin whichthemalewasencounteredwererecorded. Duringthesubsequentdays,between 10:00and 14:00.thesegmentswerechecked, allmarkedindividuals andanynewonesmarked. Intheanalysesofmaleterritorial fidelity,maleswith atleast fourrecaptures wereused forE.media Territorial characteristicsin neotropicalLibellulidae 215 andthosewith threerecapturesforMcatenataandM.hesperis.Thisdifferencein criteriawasdueto thelower frequencyofrecapturedindividuals ofthe lattertwospecies.Aperiodoffiveconsecutive dayswasused todetermine whethertheindividuals absentfromthedam foratleast onedaycould losetheirdefendedterritories. Itwasassumedthatamale hadchangeditsterritorywhen itappeared in adifferent section,notcontiguoustotheoriginally defended segment. Therelationshipbetween territorial changeand theabsenceofmaleswastestedbyaChi2analysis. RESULTS BEHAVIOUR AND TERRITORIALCHARACTERISTICS Erythrodiplax mediaseemstobemoreaggressive thantheMicrathyria species. Thefemaleswere abundantatthepond andcouples incopula wereoftenseen, butnocourtshipritualwaseverobserved.Aftercopulation, thefemalesremained forsomesecondsperched onbranchesnearthemaleterritory,generallyguarded bythemale.Finally, they oviposited neartheshorelineofthepond, inlocations withsubmerged vegetation. Oviposition was notrestricted totherespective male territories, although themalesguarded the femalesduringtheentireoviposition period, attacking othermales thatapproached. Micrathyria catenatais not avery aggressive species, though thelargest ofthe threespecies studied. Maleswereobserved, butnofemalesandmatingswereever seen. M. hesperis is asmall and likewise notvery aggressive species. A single mat- ing was observed andthere was neitheracourtship ritualnor apause between mating andoviposition. Thefemaleoviposited inthemale’sterritoryanditwas guarded by themaleflying above.However,weobservedanotherfemaleovipos- itingunguarded, perched onaleaf of Nymphea andsubmerging herabdomen. Thetwo Micrathyria species perched morefrequently onaquatic macrophytes (73.6%;n= 53), whencompared withE. mediamales, whichperched onbranch- es,grassesorevenonthesoil (78.9%; n= 19;Chi2 = 15.76;df = 1;p<0.001; Fig. 1) inadditionto using macrophytes. Comparing only Micrathyria species, M. catenataperched mainly on Eleocharis, whereas M. hesperisperched morecom- monlyon thebud oronthe leafof Nymphea (74% and48%,respectively; Chi2 = 15.34;df= 1; p<0,01; Figs lb, 1c). Theperch’s height was also differentamongthe threespecies (ANOVA; F = 12,85;df=2;p<0,01). M.catenata perched higherthanM.hesperis(Fig. 2; Tukey test; p<0,01). Theperch’s height forE.mediamaleswas intermediate, not differ- ing significantly fromthatineitherofthetwo Micrathyriaspecies(Fig.2; Tukey test;p= 0,13). Furthermore,thevegetationaroundtheterritoriesofthethreespecieswasdifferent (Chi2=50,90;df=8; p<0,01). E. mediadefendedterritorieswithEleocharisand grasses(37%and42%,respectively; Chi2= 19,89;df=4;p<0,01),whereasM. cat- enatadefendedmostlythosewithEleocharis(76%;Chi2=28,09;df= 1;p<0,01), 216 D.C. Resende&R De MarcoJr and M. hesperis thosewith Nymphea (94%;Chi: = 18,1;df = 1;p<0,01). E.mediamalesdefendedterritoriesalongtheshorelineandperched onbranch- es, grasses, directly onthe soil or on Eleocharisat anaverage height of 14cm. Thetwo Micrathyria species perched furtherover thepond thanE. media,par- ticularlyinthecaseofM. hes- peris (Chi2 = 18,83; df = 1; p<0,01)forcomparison with M. catenata (Kruskal-Wal- lis ANOVA;Chi2=21,62;df = 1; p<0,01). In M. catena- ta, thecentre of the territo- ries averaged onemeterfrom the shoreline;males perched higherthantheotherspecies, primarily on Eleocharis.The territoriesof M. hesperis ex- tendedeven furtherout over the water than those of M. catenata (Kruskal-Wallis ANOVA; Chi2 = 5,37; df = 1;p=0,021;Fig. 3)andthey mainly perched ontheleaves orflowersofNymphea.How- ever, thedistance of M. hes- peristerritoryfromtheshore- line variedand there was no homogeneity of variance in the data(Fig. 3; Bartlett Test; Chi2 = 27,128;df = 2; p<0,001). There was some differ- encein thedistancebetween perches usedby malesofthe three species (F = 11,06; df =2; p<0,01; Fig. 4). Thedis- tance between the perches used by E. media males(x =229 cm) was similarto the distancebetweenthesein M. Fig. I.Relative frequencyofthe typeofperches inViqosa, hesperis (.v = 338cm; Tukey MG.Brazil, usedby malesof:(a)E.media, —(b)M.catena- test; p=0,87). However, M. ta, - and(c) M.hesperis. catenatamalesperched near- Territorialcharacteristics inneotropicalLibellulidae 217 er theirneighbours (x = 103 cm) thanthe other two spe- cies(Tukey test; p<0,001). TERRITORIAL FIDELITY Thedisplacementof males of the three species between sectionsofthepondwassim- ilar (F = 2,24; df = 2; p = 0,13; Fig. 5).However, there- capturerate wasverylow, es- Fig. 2.Mean heightofperchesused formales ofE.media, pecially, for the Micrathyria M. catenataand M.hesperisinViijosa, MG,Brazil. Barsin- species. Ofthe 151markedE. dicate thestandard deviation. mediamalesonly35wererecaptured atleastfourtimes,whereasof the114marked M. catenataand24M. hesperis males,onlysevenandfour,respectively, werere- captured atleast threetimes. Thusonly the E. mediadatawere consideredfur- ther.Thefrequency distributionofdisplacement inthisspecies showedthatmost malesdefendedterritoriesinthesameplace,moving about 10to20meters,with onlyafewindividualsmoving morethan35meters(Fig. 6).Furthermore, in77% oftheoccasionswhenE. me- dia males stayed away from thepond foratleastone day they losttheirsectionofter- ritorialdefence, whereasthis occurred inonly 34%ofthe cases when males remained atthepond(Chi2=9,19; n= 38; df = 1;p<0,05). DISCUSSION Fig.3.Distance ofperchestothepondmargininmales ofE. Thepartition ofmicrohab- media.M. catenataand M. hesperis, in Vi?osa,MG,Brazil. itatamong the species of a pPoonsidti.veBavrasluinesd,icinattehethpeonsdta;n—danrdegdaetviviaetvioanlu.es,awayfromthe communityisacommonphe- nomenonandcan occur due to interspecific competition. Females of many Micrathyria species oviposit on aquaticplants,suchasNymphea (PAULSON, 1969),henceitishardtosaywhether themicrohabitatsselected by Micrathyria speciesas describedinthisstudy are a consequenceofcompetitionwithE.mediaora characteristicofthegenus.Libel- lulidaemostly oviposit directlyonthe surface ofthewater oronthe surfaceof wetfloating objects, including plant material— exophytic oviposition — (COR- 218 D.C. Resende& P. DeMarcoJr BET, 1999). Theoviposition on plant materialcan possi- bly result in (1) an increase in the parental care survival as theeggs wouldbeless ex- posed to predators such as fish andotheraquaticorgan- isms, or(2) adecreaseinhar- assmentoftheovipositing fe- maleby malestryingtocopu- late. Fig.4. Distance between perchesused bymales ofE.media, Males with a high degree M. catenataand M.hesperisin Viposa,MG,Brazil. Bars in- of residence should be dis- dicate thestandard deviation. placed lessoften thanmales that continually lose territo- rialdisputes(PARR, 1983;HARVEY&CORBET, 1985;CONVEY, 1989).The timeofabsenceofa territorial malefromwater canberelatedto theenergyres- torationortheperiod offoraging(FRIED& MAY,1983;ANHOLTetal., 1991; MARDEN &ROLLINS, 1994;DE MARCO, 1998). Thiscan cause confusion inthe residenceofa territory(GRIBBIN & THOMPSON, 1991), resulting ina greater displacement of residentmales.DUNHAM (1994) hasalready empha- sizedthatthe departure forforaging can makeitdifficultto maintaingood ter- ritoriesand,consequently, malescan lose matingopportunities. Nevertheless, if territorialdefencedemandsahighenergeticcost(FRIED & MAY, 1983),larger males, with larger energetic reserves, are supposed to show a higherreproduc- tivesuccess, sincethey stay fora longer timein theterritories withoutforaging (HARVEY &CORBET, 1985). The distance between in- dividualsof aspecies canbe directly relatedto the degree of aggressiveness of territo- rialmales(VAN BUSKIRK, 1986). Differences in the re- source abundancecan also affect male distribution (MEEK & HERMAN, 1991). At our locality Nym- phea covers a large area of the dam, therefore M. hes- perismalesare intheposition Fig. 5.MeanmobilityofmalesofE.media, M. catenataand toestablishterritoriesrather M. hesperisin Viyosa, MG, Brazil. Bars indicate the stand- distantfromeachother,per- ard deviation. Territorialcharacteristics inneotropicalLibellulidae 219 haps minimising therewith the intraspecific competi- tion. Nevertheless, nodiffer- enceintheresourceavailabil- ity was evident in E. media and M.catenata atthepond, the greaterdistancebetween perches in E. mediaterrito- rial males was probably due to the fact that this species performs moreaggressive in- teractions thandoes M. cat- enata. Fig. 6.Frequencydistribution ofmobilityofmarkedE.me- Thespatialarrangementof diamales inVigosa-MG,Brazil. species intohabitatunitsisacomplex resultofbionomiccharacteristics, includ- ing oviposition resources and perch choice, andinteractionswith otherspecies inthecommunity. Thebionomicfeaturesare probably themostimportant force driving thechoiceofhabitatusedby aspecies atalocality, despite thefactthat the co-occurring species can affect, atleast withincertain limits, the choiceof microhabitat. ACKNOWLEDGEMENTS We thankANDERSON LATINIforfieldassistance andTANIASANTOS, MARILIAGAIA andMARIANA MELOforvaluable revisions andcomments.Thisstudyreceived financial support fromtheBrazilian Conselho Nacional dePesquisas(CNPq). REFERENCES ALCOCK,X, 1987a.Malereproductivetacticsinthelibellulid dragonflyPaltothemislineatipes:tem- poralpartitioningofterritories.Behaviour 103: 157-173. ALCOCK,J., 1987b.Theeffectsofexperimentalmanipulationofresourcesonthebehavior oftwoca- lopterygid damselfliesthat exhibit resource-defense polygyny. Can.J.Zool. 65: 2475-2482. ANHOLT, B.R.,J.H.MARDEN&D.M.JENKINS, 1991.Patterns ofmassgainandsexualdimor- phismin adultdragonflies(Insecta:Odonata).Can. J.Zool. 69; 1156-1163. BATTIN,T.X, 1993. The odonate matingsystem,communication,and sexual selection: areview. Boll. Zool. 60: 353-360. CONVEY,P, 1989.Influencesonthechoicebetween territorial andsatellitebehaviourinmaleLibel- lulaquadrimaculataLinn.(Odonata;Libellulidae).Behaviour 109: 125-141. CORBET, P.S., 1999. Dragonflies: behavior andecologyofOdonata. Comstock Publ. Assoc,, Ith- aca,NY. DEMARCO,P.,Jr, 1998. TheAmazonian Campinadragonflyassemblage:patternsinmicrohabitat useand behavior inaforaginghabitat. Odonatologica27;239-248. DEMARCO,P,Jr&D.C.RESENDE, 2004.Cues forterritorychoice intwotropicaldragonflies. Neotrop.Ent. 33: 397-401. 220 D.C. Resende&P.De MarcoJr DUNHAM,M„1994. Theeffectofphysicalcharacters onforaginginPachydiplax longipennis(Bur- meister)(Anisoptera:Libellulidae).Odonatologica23: 55-62. FRIED,C.S.&ML.MAY, 1983.Energyexpenditureandfood intakeofterritorial malePachydiplax longipennis(Odonata:Libellulidae).Ecol. Ent.8:283-292. GOLFARI,L., 1975.Zoneamenloecoldgico doEstadode MinasGeraispararefloreslamenlo.CPRFC, Belo Horizonte,MG. GRIBBIN,S.D.&D.J. THOMPSON, 1991.Theeffectsofsizeandresidency onterritorial disputes andshort-term matingsuccessin thedamselflyPyrrhosomanymphula(Sulzer)(Zygoptera: Coenagrionidae).Anim. Behav. 41:689-695. HARVEY, I.F.& RS. CORBET, 1985. Territorial behaviour oflarvaeenhances matingsuccessof maledragonflies.Anim.Behav. 33: 561-565. HASSAN,A.T., 1978.ReproductivebehaviourofAcisomapanorpoidesinflatumSelys(Anisoptera: Libellulidae).Odonatologica7:237-245. JOHANNSSON,O.E., 1978.Co-existenceoflarvalZygopteracommontotheNorfolk Broads(U.K.), 1.Temporalandspatialseparation.Oecologia 32; 303-321. 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