ebook img

Distribution of Brachypelma vagans (Theraphosidae) burrows and their characteristics in Belize over two years PDF

2011·2.6 MB·English
Save to my drive
Quick download
Download
Most books are stored in the elastic cloud where traffic is expensive. For this reason, we have a limit on daily download.

Preview Distribution of Brachypelma vagans (Theraphosidae) burrows and their characteristics in Belize over two years

2011.TheJournalofArachnology39:515-518 SHORT COMMUNICATION Distribution ofBmchypebmi vagam (Theraphosidae) burrows and their characteristics in Belize over two years Emma M. Shaw, Susan P. Bennettand C. PhilipWheater: Department ofEnvironmental and Geographical Sciences, Manchester Metropolitan University, Manchester, M15 5GD, UK. E-mail: [email protected] Abstract. To help to address the paucity ofecological knowledge available for Brachypelnui vagansAusserer 1875, a CITESprotectedspecies,wemonitoredapopulationinWesternBelizefortwoyearstoprovidedatafordistributionand dispersal.Despitepreviousover-collectionforthepettrade,thespeciesislocallyhighlyabundantinsomeareasofBelize. Werecordedthedistribution,burrowandspidercharacteristicsofB. vagansin2007and2008atLasCuevasResearch Station, Belize. Populationdynamicswerecompared betweenyears,aswasindividual location. Over 100burrowswere locatedinbothyears;however,previousassumptionsthatindividualsdonotmoveburrowsregularlyappearnegated,since only12burrowlocationsmatchedbetweenyears,suggestinghighintra-habitatdispersal.Despitethisapparenthighlevelof movement burrows were significantly clumped, to a similar degree, in both years. This movement could be due to disturbancesthroughouttheyear,includingHoodingduringtherainyseason.Burrowsizecorrelatedwithindividualbody size,exceptinafewjuvenilesthatappeartohaveopportunisticallyclaimedanemptyburrow,accountingforsomesmall animalsfoundinlargeburrows. Keywords: Burrow,Belize,ecology,red-rumptarantula,populationstructure Brachypelma vagansAusserer 1875 isoneofthemost ubiquitous currentstudyexaminesthepopulationdynamicsanddistributionof BrachypelnuispeciesofNeotropicallowlandforesthabitats.Asthese one B. vagans population for two consecutive years to elucidate tarantulasarelonglived,brightlycoloured,andusuallydocile,they patternsofmovementandactivityandprovidean understandingof arepopularpetsandsufferfromover-harvesting,nowbeinglistedas thehabitatrequirementsandpopulationpressuresonthespecies. threatenedCITIESAppendixIIspecies(Petersonetal.2006).Despite Thetechniquesusedoverthetwoyearswereidentical.Thestudy B. vagans having the widest distribution of Brachypelnui species siteatLasCuevasResearchStation,Chiquibulrainforestarea,Cayo (being recorded from Mexico, Belize and other parts of Central district,Belize(GPSlocation88°59.188'W, 16°43.990'N,elev.583m) America:Reichling 1999),thereislimitedinformationonitsecology is classified as lowland tropical broad-leafed rain forest, which and habitat preferences (e.g., Yanez & Floater 2000; Henaut & stretches from the Caribbean coast ofMexico, through Belize and Machkour-M’Rabet2005;Machkour-M’Rabetetal.2007;Doretal. into Honduras and the Peten region of Guatemala. The study 2008),withmoststudiesonBrachypelnuitarantulasconcerningtheir populationofB. vagansisintheclearing(150x 121 m)surrounding geographic distributions (Valerio 1980; Smith 1986; Edwards & research station buildings, which are mainly to the south side (the Hibbard 1999; Locht et al. 1999), systematics (Coddington & Levi currentresearchconcentratedonthenorthsideoftheclearing:98 X 1991; Perez-Miles et al. 1996) and genetics (Longhorn 2002; 121m).Belttransects(1mwide)werelaidperpendiculartotheback Longhorn et al. 2007; Machkour-M'Rabet et al. 2009). The rarity oftheclearing(whereitmetforestundergrowth)andsystematically ofsomeBrachypelmaspecies(e.g.,Yanez&Eloater2000),combined searchedforsignsofburrows,whichwerelabelledusinganumbered withhabitatdegradationandillegalcaptureandtrade, suggeststhe fiag to enable easy relocation at night, when individuals were needforcaptivebreedingpriortoreintroduction(Yanezetal. 1999). extracted for measurement. The location of each burrow and its Itisessentialtherefore,toobtaindetailedknowledgeoftheirhabitat openingdimensions(usingthewidestwidthandlongestlengthofthe requirements and changes within populations to provide a greater mouth)wererecorded. The surveys took place in June and July in understandingofthefactorsinfluencingtheirspatialdistributionand both2007and2008. populationdynamics. Visitingburrowsatnightwhenindividualssatattheburrowmouth Brachypelmavagansconstructburrowswithsingleentranceswhere gaveaclearindication ofoccupancyand helped to minimizestress they spend the day, spinning silk around the entrance to transmit when removing animals using a fishing technique (Reichling 2003) vibrationsfrom preymovements(Yanez& Floater2000). Theyare involvingabladeofgrasswavedtomimicpreymovements.Oncethe nocturnal predators feeding mainly on ground-dwelling arthropods individualwasremoved,theentrancewasblockedandtheindividual andpossiblysmallvertebrates(Marshall 1996). Machkour-M’Rabet placedinaclearplasticbagtoallowmanipulationandmeasurement. etal.(2007)founddensitiesofB. vaganstobehigherinopenrather Whenindividualswerenotseen,theburrowwasmonitoredforsigns thanforestsitesandwithhighdensitiesofburrowscharacterisedby ofoccupancy(e.g.,silkandsoilextractedfromtheburrow). deepclayishsoils,whichisunsurprisinggiventhatindividuals,onthe The minimum distance between burrows was calculated using whole,digtheirownburrows.Littleisknownaboutburrowfidelity trigonometry, and aggregation between burrowswasassessed using and which factors cause burrow relocation, although some field nearestneighbouranalysis(e.g., Wheateret al. 2011). Theindexof observations suggest that females locate occupied burrows of aggregation was calculated as the ratio between the mean and the conspecifics and attack and consume the residents (Henaut & expecteddistancesbetweenburrows(wheretheexpecteddistancewas Machkour-M’Rabet, 2005). Lack of long-term distributional data estimatedas: l/[2vdensity]). Independentsamples/-testswereusedto foranyB.vaganspopulationposesdifficultiesindeterminingthelevel examine differences in nearest neighbor distances between years to ofintra-populationmovement,whetherburrowswappingoccurs,or determinewhetherclusteringdiffers between years (see Krebs 1999 thedistancesthatindividualsmovetofind,ordig,anewburrow.The for a fuller explanation ofnearest neighbor analysis). A Pearson’s 515 516 THEJOURNALOFARACHNOLOGY — Figure 1. Schematicrepresentationofthelocationofallburrowslocatedin2007and2008onthenorthsideoftheLasCuevasResearch Stationclearing.Theclearingboundaries,pathandbuildingsandfloodzoneareallshownforreference(shadedareas). product moment correlation coefficient was used to determine burrowstructureasB. vcigaiiscanhaveuptofourchambersoffthe relationships between spider and burrow size, for all caught main burrow (Machkour-M’Rabet et al. 2007) and be recorded at individuals,ineachyear. depthsof3-40cm(Machkour-M’Rabetetal.2007)andupto50cm Over 100burrowswerelocated(108in2007and 107 in2008),of (Shawpers.obs.).Rainfallcanbehighduringthewetseason,andthe which 80wereoccupied in 2007, and 73 in 2008. More individuals clearingissubjecttoseasonalHooding,which,coupledwiththelack wereextractedin2007(48comparedto26in2008),andtherewasa of deep roots, could lead to burrow collapse. Of those burrows higher percentage ofjuveniles in 2007 (41%) than in 2008 (7%). matchingbetween2007and2008somewereprotectedfromcollapse, Despitethesimilarity in burrow numbersfound in bothyears, it is being underneath the edges of buildings, rocks and large roots. evidentfromFig. I thattheirdistributionismarkedlydifferentwith Burroworientationcanmakethemmoresusceptibletorain-carrying aonrloyun1d2bpurielsdeinntgsfraonmdo1nyetahreetodgtehseonfexatc.onMcarnetyebpuatrhr.owAslwaerrgeenluomcabteerd w20i0n5d)s,,hbeultpilnegadtiongmaitontaaintrhaidge-hofhfumbiedtiwteye(nMaocphtkiomuurm-Mh’uRmaibdiettyetanald. of burrows were found in the west side of the clearing in 2007, having to movewhen flooded. Certainly areas that regularly flood whereasin2008theproportionpresentinthisareawasreduced.An havealmostnoburrows,andthoseattheedgeofthefloodzonecan areapronetofloodinghadfewburrowspresentineitheryear(Fig. 1). become waterlogged, resulting in tarantulas sitting huddled at the Therewasnosignificantdifferencebetweenmeannearestneighbour mouth ofthe burrow until the water subsides. Repeated flooding distancesbetweenburrowsin2007and2008(f= 1.658,df=213,F= couldresultinabandonment,asobservedinotherburrowingspiders 0m.)0.99B;u2r0r0o7w:smweearne=sig3n.i8f8ic(aSnEtl=yc0l.3u1m)pme;d2i0n08b:otmhea20n07=3(.Z16=(S4.E43=,0d.f27=) j(uMvaernsilheasl,lpo1s9s95i)b.lyAebxapnladionninegdtbheurrloowwscowroruelladtiotnhebnetbweeenfresepidfeorr 107, P< 0.0001)and2008 (Z= 7.23,df= 106, P< 0.0001),with stageandburrowsize. similarindicesofaggregation(2007:1,4 =0.64;2008:Ia =0.60).For The nearest neighbour analysis showed similar mean distances occupied burrows, there was no significant difference between the betweenburrowsintheNorthofBelize,asfoundbyReichling(1999: nearest neighbourdistancesbetweenyears(t = 1.02,df= 152, R = 3.4 m), and those at Las Cuevas (3.88 m, 2007; 3.16 m, 2008), 0.331; Table 1). In both years, occupied burrows were significantly suggesting that there may be an optimal distance driven by clumped(2007:1,4 =0.77,Z=4.43,df=79,P<0.0001;2008:Ia = competitive repulsion (Reichling 1999). The level ofbetween-year 0.70,Z=5.41,df=72,P<0.0001).However,thespatialdistribution movementimpliedbythisstudymaybeduetorelocationofjuveniles ofburrowsdifferedbetweenyears(Fig. 1)withthosecontainingadults priorto reachingmaturity. Machkour-M’Rabet et al. (2005)found being more clustered than those with juveniles, and areas where thatadultsandjuvenilesaggregatedseparately,althoughthisisnot burrowswerefoundinoneyearbutnotintheother. evident in the study population. Reichling (1999) suggests that Foreachyear,theoccupiedburrowsizewassignificantlypositively aggregative tendencies in theraphosids could reduce exposure to correlated with spider body length (2007: r = 0.376, n = 48, F = predatorsandincreasereproductivesuccessofnomadicmalesdueto 0.008; 2008: r = 0.424, n = 26, P = 0.031; Fig.2), and in general theshorterroamingdistancesrequiredbetweenfecundfemales.This largerspiderswerefoundinlargerburrowswithsomeexceptionsof can further be aided by the presence ofdetectable chemical cues small juveniles inhabiting what appeared to be abandoned adult (Yanezetal. 1999). burrows. Dor et al. (2008) found females readily enter burrows ofother Despitesimilarnumbersofburrowsbeingfoundinbothyears,the females,sometimesresultingintheattackanddeathofoneofthem locationsweremarkedlydifferent, suggestingthat individualsmove (Henaut and Machkour-M’Rabet 2005). With high densities and betweenpre-existingburrowsortonewburrows.Examinationofthe clustered burrows, it is possible that there is frequent burrow clearing in 2008 revealed no visible signs ofold burrows in areas takeover, particularly since chemical cues left by the silk at the where burrows had previously been present. This could be due to burrowmouthcanattractfemalestoeachother(Doretal.2008). SHAWETAL.—DISTRIBUTIONOFBRACHYPELMA VAGANSBURROWS 517 — Figure 2. CorrelationbetweenthebodysizeofB. vagcmstarantulasandthewidthoftheirburrowsatLasCuevasResearchStation,Belizein 2007and2008. Inconclusion,thisstudyhighlightsthatthepopulationofB.vagcmsat Locht, A., M. Yanez& 1. Vasquez. 1999. Distribution and natural LasCuevasResearchStationisstableandhighlymobile.In2007much history of Mexican species of Brachypelma and Bruchypelmicles ofthecapturedpopulationwascomposedofjuveniles,whereasin2008 (Theraphosidae,Theraphosinae)withmorphologicalevidencefor more were adults, suggesting that the population is developing and theirsynonymy.JournalofArachnology27:196-200. indicatingapotentialpopulationboomasthelargenumberofadults Longhorn, S.J. 2002. Non-lethal DNA sampling from CITES II producejuveniles.Ifthisisthecase,continuedstudiesonthispopulation protected‘tarantula’spidersofBelize.LasCuevasNewsletter9:8-9. shouldhelpelucidatesomepatternsofdispersalanddistribution. Longhorn, S.J., M. Nicholas, J. Chuter & A.P. Volger. 2007. The ACKNOWLEDGMENTS utilityofmolecularmarkersfromnon-lethalDNAsamplesofthe CITES II protected “tarantula” Bracypelma vagans (Araneae, TheauthorswouldliketothankallthestudentsontheManchester Theraphosidae).JournalofArachnology35:278-292. Metropolitan University and the University of Manchester Belize Machkour-M’Rabet.S.,Y.Hennaut,R.Roberto&S.Calme.2005.Anot fieldcourse, VickyOgilvy, whoassistedwith collectingindividuals, so natural history ofthetarantula Brachypelma vagan.s\ Interaction andLasCuevasResearchStationandtheBelizeForestryDepartment withhumanactivity.JournalofNaturalHistory39:2515-2523. forallowingthisworktobeconducted. Machkour-M’Rabet, S., Y. Hennaut, A. Sepulveda, R. Rojo, S. LITERATURECITED Clame&V.Geissen.2007.Soilpreferenceandburrowstructureof an endangered tarantula, Brachypelma vagans (Mygalomorphae; Coddington,J.A. & H.W. Levi. 1991. Systematicsandevolution of Theraphosidae).JournalofNaturalHistory41:1025-1033. spiders (Araneae). Annual Review of Ecology and Systematics Machkour-M’Rabet,S.,Y. Hennaut,A. Dor,G. Perez-Lachaud,C. 22:565-592. Pelissier,C. Gers&L. Legal. 2009. ISSR(InterSimpleSequence Dor,A.,S.Machkour-M’Rabet,L.Legal,T.Williams&Y.Henaut.2008. Repeats) as molecular markers to study genetic diversity in Chemicallymediatedburrowrecognitition inthe Mexican tarantula Tarantulas(Mygalomorphae).JournalofArachnology37:10-14. Brachypelmavagansfemale.Naturwissenschaften95:1189-1193. Marshall, S.D. 1995. Mechanisms of the formation of territorial Edwards, G.B. & L.H. Hibbard. 1999. The Mexican redrump, aggregationsoftheburrowingwolfspiderGeolyco.saxeraarchhokU Brachypelmavagans(Araneae; T/ieraphosidae),anexotictarantula McCrone(Araneae,Lycosidea).JournalofArachnology23:145-150. established in Florida. Entomology Circular394. Department of Marshall, S.D. 1996. Evidence for territorial behaviour in a Agriculture & Consumer Services, Division of Plant Industry, burrowingwolfspider.Ethology 102:32-39. Gainesville,Florida. Perez-Miles, F., S.M. Lucas, P.I. da Silva, Jr. & R. Bertani. 1996. Henaut, Y. & S. Machkour-M’Rabet. 2005. Canibalismo y clepto- Systematic revision and dadistic analysis of Theraphosinae biosisen latarantula Brachypelma vagans. Entomology Mexican (Araneae:Theraphosidae). Mygalomorph 1:33-68. 4:30-32. Peterson,S.D.,T.Mason,S.Akbar,R.West,B.White&P.Wilson.2006. Krebs, C.J. 1999. Ecological Methodology, 2nd Edition. Addison- Species identification of tarantulas using exuviae for international WesleyEducationalPublishers,NewYork. wildlifelawenforcement.ConservationGenetics8:497-502. 518 THEJOURNALOFARACHNOLOGY Reichling, S.B. 1999. Spatial relationshipsoftheraphosidspidersin Wheater, C.P., J.R. Bell & P.A. Cook. 2011. Practical Field Belize.SouthwesternNaturalist4.5:518-521. Ecology:AProjectGuide.Wiley-Blackwell,London. Reichling,S.B.2000.GroupdispersalinjuvenileBrachypelmavagcms Yaiiez, M., A. Locht & R. Marcias-Ordonez. 1999. Courtshipand (Araneae,Theraphosidae).JournalofArachnology28:248-250. matingbehaviorofBrachypelmaklaasi(Araneae,Theraphosidae). Reichling, S.B. 200.5. Tarantulas of Belize. Krieger Publishing JournalofArachnology27:165-170. Company,Malabar,Florida, Yanez, M. & G. Floater. 2000. Spatial distribution and habitat Smith, A. 1986. The Tarantula: Classification and Identification preference of the endangered tarantula, Brachypelma klaasi Guide. FitzgeraldPublishing, London. (Araneae:Theraphosidae)in Mexico. BiodiversityandConserva- Valerio, C. 1980. Aranas Terafosidas de Costa Rica (Araneae: tion9:795-810. Theraphosidae). 1.SericopehnayBrachypelma. Brenesia 18:288. Manuscriptreceived11June2010, revised22September2011.

See more

The list of books you might like

Most books are stored in the elastic cloud where traffic is expensive. For this reason, we have a limit on daily download.