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Site fidelity and patterns of short- and long-term movement in the brilliant-thighed poison frog Allobates femoralis (Aromobatidae)

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Abstract

We studied movement and site fidelity of males and females of the territorial frog Allobates femoralis (Aromobatidae) in a population in the Nature Reserve “Les Nouragues” in French Guiana, South America. Observations during 3 months in 2006 ascertained intra-seasonal site fidelity for males and females. Males actively defend large multi-purpose territories whereas females retreat to small resting sites from where they commute to neighbouring males for courtship and mating. Female short-term movement corroborates the previous assumption of a polygynous or promiscuous resource-defence mating system. Year-to-year recaptures from 2005 until 2008 revealed distinct patterns of inter-annual movement for males and regional site fidelity for females. Males abandon their territories and have to re-negotiate them when reproduction starts again at the end of the dry season. Females are not subject to intra- or inter-sexual territorial competition and as a result move significantly less between reproductive seasons than males. Male long-term movement reflects spatial structure and prevailing social interactions and is a reliable indicator for tadpole deposition sites. The combined effects of intra- and inter-seasonal movement promote the diversity of mates for both sexes.

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References

  • Aichinger M (1991) Tadpole transport in relation to rainfall, fecundity, and body size in five species of poison-dart frogs from Amazonian Peru. Amphib–Reptil 12:49–55. doi:10.1163/156853891X00329

    Google Scholar 

  • Amézquita A, Hödl W, Lima AP, Castellanos L, Erdtmann L, de Araújo MC (2006) Masking interference and the evolution of the acoustic communication system in the Amazonian dendrobatid frog Allobates femoralis. Evolution 60:1874–1887. doi:10.1554/06-081.1

    PubMed  Google Scholar 

  • Andreone F (1998) Capture–recapture study of Mantidactylus microtympanum (Anura, Ranidae, Mantellinae) from the Andohahela low altitude rainforest, south-eastern Madagascar. Amphib–Reptil 19:451–455. doi:10.1163/156853898X00142

    Google Scholar 

  • Arak A (1983) Male–male competition and mate choice in anuran amphibians. In: Bateson P (ed) Mate choice. Cambridge University Press, Cambridge, pp 181–210

    Google Scholar 

  • Bee MA (2007) Selective phonotaxis by male wood frogs (Rana sylvatica) to the sound of a chorus. Behav Ecol Sociobiol 61:955–966. doi:10.1007/s00265-006-0324-8

    Article  Google Scholar 

  • Beyer HL (2004) Hawth’s analysis tools for ArcGIS. Version 3.26 http://www.spatialecology.com/htools

  • Bollinger EK, Switzer PV (2002) Modeling the impact of edge avoidance on avian nest densities in habitat fragments. Ecol Appl 12:1567–1575. doi:10.2307/3099922

    Article  Google Scholar 

  • Born MG, Gaucher P (2001) Distribution and life histories of amphibians and reptiles. In: Bongers F, Charles-Dominique P, Forget P, Théry M (eds) Nouragues. Dynamics and plant–animal interactions in a neotropical rainforest. Kluwer Academic, Dordrecht, pp 167–184

    Google Scholar 

  • Bosch J, De la Riva I (2004) Are frog calls modulated by the environment? An analysis with anuran species from Bolivia. Can J Zool 82:880–888. doi:10.1139/z04-060

    Article  Google Scholar 

  • Boyé M, Cabaussel G, Perrot Y (1979) Climatologie. In: Lasserre G, Sautter G, Boyé M, Brasseur G (eds) Atlas des départements français d’Outre-Mer: 4. La Guyane. CNRS/ORSTOM, Paris

    Google Scholar 

  • Butler D (2006) Murders halt rainforest research. Nature 441:555. doi:10.1038/441555a

    Article  PubMed  CAS  Google Scholar 

  • Chiu C, Kam Y (2006) Testing the nest-homing abilities of a phytotelm-breeding frog, Chirixalus eiffingeri (Rhacophoridae). Zool Sci 23:501–505. doi:10.2108/zsj.23.501

    Article  PubMed  Google Scholar 

  • Crump ML (1986) Homing and site fidelity in a neotropical frog, Atelopus varius (Bufonidae). Copeia 1986:438–444. doi:10.2307/1445001

    Article  Google Scholar 

  • Crump ML (1988) Aggression in harlequin frogs: male–male competition and a possible conflict of interest between the sexes. Anim Behav 36:1064–1077. doi:10.1016/S0003-3472(88) 80066-6

    Article  Google Scholar 

  • Dall SRX, Giraldeau L, Olsson O, McNamara JM, Stephens DW (2005) Information and its use by animals in evolutionary ecology. Trends Ecol Evol 20:187–193. doi:10.1016/j.tree.2005.01.010

    Article  PubMed  Google Scholar 

  • Data East (2003–2007) XTools Pro for ArcGIS desktop. Version 4.2.0 (Build 383). Data East, Novosibirsk

    Google Scholar 

  • De Solla SR, Bonduriansky R, Brooks RJ (1999) Eliminating autocorrelation reduces biological relevance of home range estimates. J Anim Ecol 68:221–234. doi:10.1046/j.1365-2656.1999.00279.x

    Article  Google Scholar 

  • Diego-Rasilla FJ, Luengo RM, Phillips JB (2005) Magnetic compass mediates nocturnal homing by the alpine newt, Triturus alpestris. Behav Ecol Sociobiol 58:361–365. doi:10.1007/s00265-005-0951-5

    Article  Google Scholar 

  • Dole JW, Durant P (1974) Movements and seasonal activity of Atelopus oxyrhynchus (Anura: Atelopodidae) in a Venezuelan Cloud Forest. Copeia 1974:230–235. doi:10.2307/1443028

    Article  Google Scholar 

  • Donnelly MA (1989a) Effects of reproductive resource supplementation on space-use patterns in Dendrobates pumilio. Oecologia 81:212–218. doi:10.1007/BF00379808

    Google Scholar 

  • Donnelly MA (1989b) Demographic effects of reproductive resource supplementation in a territorial frog, Dendrobates pumilio. Ecol Monogr 59:207–221. doi:10.2307/1942599

    Article  Google Scholar 

  • Donnelly MA, Guyer C, Juterbock JE, Alford RA (1994) Techniques for marking amphibians. In: Heyer WR, Donnelly MA, McDiarmid RW, Hayek LC, Foster MS (eds) Measuring and monitoring biological diversity. Standard methods for amphibians. Smithsonian Institution, Washington, DC, pp 277–284

    Google Scholar 

  • Doty GV, Welch AM (2001) Advertisement call duration indicates good genes for offspring feeding rate in gray treefrogs (Hyla versicolor). Behav Ecol Sociobiol 49:150–156. doi:10.1007/s002650000291

    Article  Google Scholar 

  • ET SpatialTechniques (2007) ET Geo Wizards. Version 9.6.1. ET SpatialTechniques, Pretoria

    Google Scholar 

  • Ferguson DE, McKeown JP, Bosarge OS, Landreth HF (1968) Sun-compass orientation of bullfrogs. Copeia 1968:230–235. doi:10.2307/1441746

    Article  Google Scholar 

  • Forester DC, Wisnieski A (1991) The significance of airborne olfactory cues to the recognition of home area by the dart-poison frog Dendrobates pumilio. J Herpetol 25:502–504. doi:10.2307/1564782

    Article  Google Scholar 

  • Forester DC, Snodgrass JW, Marsalek K, Lanham Z (2006) Post-breeding dispersal and summer home range of female American toads (Bufo americanus). Northeast Nat 13:59–72. doi:10.1656/1092-6194(2006) 13[59:PDASHR]2.0.CO;2

    Article  Google Scholar 

  • Forsman A, Hagman M (2006) Calling is an honest indicator of paternal genetic quality in poison frogs. Evolution 60:2148–2157. doi:10.1554/06-258.1

    PubMed  Google Scholar 

  • Gascon C (1991) Population- and community-level analyses of species occurrences of central Amazonian rainforest tadpoles. Ecology 72:1731–1746. doi:10.2307/1940972

    Article  Google Scholar 

  • Gasser H, Amézquita A, Hödl W (2009) Who is calling? Intraspecific call variation in the aromobatid frog Allobates femoralis. Ethology 115:596–607

    Article  Google Scholar 

  • Göd M, Franz A, Hödl W (2007) The influence of internote-interval variation of the advertisement call on the phonotactic behaviour in male Allobates femoralis (Dendrobatidae). Amphib–Reptil 28:227–234. doi:10.1163/156853807780202468

    Google Scholar 

  • Gottsberger B, Gruber E (2004) Temporal partitioning of reproductive activity in a neotropical anuran community. J Trop Ecol 20:271–280. doi:10.1017/S0266467403001172

    Article  Google Scholar 

  • Greenwood PJ, Harvey PH (1982) The natal and breeding dispersal of birds. Ann Rev Ecolog Syst 13:1–21. doi:10.1146/annurev.es.13.110182.000245

    Article  Google Scholar 

  • Grimaldi M, Riéra B (2001) Geography and climate. In: Bongers F, Charles-Dominique P, Forget P, Théry M (eds) Nouragues. Dynamics and plant–animal interactions in a neotropical rainforest. Kluwer Academic, Dordrecht, pp 9–18

    Google Scholar 

  • Haase A, Pröhl H (2002) Female activity patterns and aggressiveness in the strawberry poison frog Dendrobates pumilio (Anura: Dendrobatidae). Amphib–Reptil 23:129–140. doi:10.1163/156853802760061778

    Google Scholar 

  • Harvey MJ, Barbour RW (1965) Home range of Microtus ochrogaster as determined by a modified minimum area method. J Mammal 46:398–402. doi:10.2307/1377624

    Article  Google Scholar 

  • Heying HE (2001) Social and reproductive behaviour in the Madagascan poison frog, Mantella laevigata, with comparisons to the dendrobatids. Anim Behav 61:567–577. doi:10.1006/anbe.2000.1642

    Article  Google Scholar 

  • Hödl W (1983) Phyllobates femoralis (Dendrobatidae): Rufverhalten und akustische Orientierung der Männchen (Freilandaufnahmen). Wiss Film 30:12–19 Bundesstaatliche Hauptstelle für Wissenschaftliche Kinematographie, Vienna

    Google Scholar 

  • Hödl W, Amézquita A, Narins PM (2004) The role of call frequency and the auditory papillae in phonotactic behavior in male dart-poison frogs Epipedobates femoralis (Dendrobatidae). J Comp Physiol A 190:823–829. doi:10.1007/s00359-004-0536-1

    Article  Google Scholar 

  • Ihara Y (2002) A model for evolution of male parental care and female multiple mating. Am Nat 160:235–244. doi:10.1086/341019

    Article  PubMed  Google Scholar 

  • Juncá FA, Eterovick PC (2007) Feeding ecology of two sympatric species of Aromobatidae, Allobates marchesianus and Anomaloglossus stepheni, in central Amazon. J Herpetol 41:301–308. doi:10.1670/0022-1511(2007) 41[301:FEOTSS]2.0.CO;2

    Article  Google Scholar 

  • Lescure J (1976) Etude des têtards de deux Phyllobates (Dendrobatidae). Bull Soc Zool Fr 101:299–306

    Google Scholar 

  • Lima AP, Magnusson WE (1998) Partitioning seasonal time: interactions among size, foraging activity and diet in leaf-litter frogs. Oecologia 116:259–266. doi:10.1007/s004420050587

    Article  Google Scholar 

  • Luger M (2006) Wanted: riverside home—habitat association in male harlequin toads (Atelopus hoogmoedi, Bufonidae) from Suriname. M.Sc. thesis, Department of Evolutionary Biology, University of Vienna, Vienna

  • Magaña Mendoza D (2008) Territory size in Allobates femoralis (Dendrobatidae): playback versus observational method. M.Sc. thesis, Department of Evolutionary Biology, University of Vienna, Vienna

  • Mardia KV, Jupp PE (2000) Directional statistics (Wiley series in probability and statistics). Wiley, Chichester

    Google Scholar 

  • Marsh DM (2001) Fluctuations in amphibian populations: a meta-analysis. Biol Conserv 101:327–335. doi:10.1016/S0006-3207(01) 00076-3

    Article  Google Scholar 

  • McVey ME, Zahary RG, Perry D, MacDougal J (1981) Territoriality and homing behavior in the poison dart frog (Dendrobates pumilio). Copeia 1981:1–8. doi:10.2307/1444035

    Article  Google Scholar 

  • Miaud C, Sanuy Castells D, Avrillier J (2000) Terrestrial movements of the natterjack toad Bufo calamita (Amphibia, Anura) in a semi-arid, agricultural landscape. Amphib–Reptil 21:357–369. doi:10.1163/156853800507426

    Google Scholar 

  • Narins PM, Hödl W, Grabul DS (2003) Bimodal signal requisite for agonistic behavior in a dart-poison frog, Epipedobates femoralis. PNAS 100:577–580. doi:10.1073/pnas.0237165100

    Article  PubMed  CAS  Google Scholar 

  • Narins PM, Grabul DS, Soma KK, Gaucher P, Hödl W (2005) Cross-modal integration in a dart-poison frog. PNAS 102:2425–2429. doi:10.1073/pnas.0406407102

    Article  PubMed  CAS  Google Scholar 

  • Orgutsov SV (2004) Olfactory orientation in anuran amphibians. Russ J Herpetol 11:35–40

    Google Scholar 

  • Otter K, McGregor PK, Terry AMR, Burford FRL, Peake TM, Dabelsteen T (1999) Do female great tits (Parus major) assess males by eavesdropping? A field study using interactive song playback. Proc R Soc Lond B 266:1305–1309. doi:10.1098/rspb.1999.0779

    Article  Google Scholar 

  • Pasinelli G, Müller M, Schaub M, Jenni L (2007) Possible causes and consequences of philopatry and breeding dispersal in red-backed shrikes Lanius collurio. Behav Ecol Sociobiol 61:1061–1074. doi:10.1007/s00265-006-0339-1

    Article  Google Scholar 

  • Passmore NI, Telford S (1981) The effect of chorus organization on mate localization in the painted reed frog (Hyperolius marmoratus). Behav Ecol Sociobiol 9:291–293. doi:10.1007/BF00299885

    Article  Google Scholar 

  • Patrick DA, Calhoun AJK, Hunter ML JR (2007) Orientation of juvenile wood frogs, Rana sylvatica, leaving experimental ponds. J Herpetol 41:158–163. doi:10.1670/0022-1511(2007)41[158:OOJWFR]2.0.CO;2

    Article  Google Scholar 

  • Payne RB, Payne LL (1993) Breeding dispersal in indigo buntings: circumstances and consequences for breeding success and population structure. Condor 95:1–24. doi:10.2307/1369382

    Article  Google Scholar 

  • Pellet J, Rechsteiner L, Skrivervik AK, Zürcher J, Perrin N (2006) Use of the harmonic direction finder to study the terrestrial habitats of the European tree frog (Hyla arborea). Amphib–Reptil 27:138–142. doi:10.1163/156853806776052173

    Google Scholar 

  • Poelman EH, Dicke M (2008) Space use of Amazonian poison frogs: testing the reproductive resource defense hypothesis. J Herpetol 42:270–278

    Article  Google Scholar 

  • Poncy O, Sabatier D, Prévost M, Hardy I (2001) The lowland high rainforest: structure and tree species diversity. In: Bongers F, Charles-Dominique P, Forget P, Théry M (eds) Nouragues. Dynamics and plant–animal interactions in a neotropical rainforest. Kluwer Academic, Dordrecht, pp 31–47

    Google Scholar 

  • Pope KL, Matthews KR (2001) Movement ecology and seasonal distribution of mountain yellow-legged frogs, Rana muscosa, in a high-elevation Sierra Nevada basin. Copeia 2001:787–793. doi:10.1643/0045-8511(2001) 001[0787:MEASDO]2.0.CO;2

    Article  Google Scholar 

  • Pröhl H (2003) Variation in male calling behaviour and relation to male mating success in the strawberry poison frog (Dendrobates pumilio). Ethology 109:273–290. doi:10.1046/j.1439-0310.2003.00863.x

    Article  Google Scholar 

  • Pröhl H (2005) Territorial behavior in dendrobatid frogs. J Herpetol 39:354–365. doi:10.1670/162-04A.1

    Article  Google Scholar 

  • Robertson JGM (1984) Acoustic spacing by breeding males of Uperoleia rugosa (Anura: Leptodactylidae). Z Tierpsychol 64:283–297

    Google Scholar 

  • Roithmair ME (1992) Territoriality and male mating success in the dart-poison frog, Epipedobates femoralis (Dendrobatidae, Anura). Ethology 92:331–343

    Article  Google Scholar 

  • Roithmair ME (1994) Field studies on reproductive behaviour in two dart-poison frog species (Epipedobates femoralis, Epipedobates trivittatus) in Amazonian Peru. Herpetol J 4:77–85

    Google Scholar 

  • Santos EM, Almeida AV, Vasconcelos SD (2004) Feeding habits of six anuran (Amphibia: Anura) species in a rainforest fragment in northeastern Brazil. Iheringia Sér Zool 94:433–438. doi:10.1590/S0073-47212004000400014

    Google Scholar 

  • Silverstone PA (1976) A revision of the poison-arrow frogs of the genus Phyllobates Bibron in Sagra (Family Dendrobatidae). Nat Hist Mus Los Angeles Co Sci Bull 27:1–53

    Google Scholar 

  • Simões PI, Lima AP, Magnusson WE, Hödl W, Amézquita A (2008) Acoustic and morphological differentiation in the frog Allobates femoralis: relationships with the upper Madeira River and other potential geological barriers. Biotropica 40:607–614. doi:10.1111/j.1744-7429.2008.00416.x

    Article  Google Scholar 

  • Sinsch U (1988) Seasonal changes in the migratory behaviour of the toad Bufo bufo: direction and magnitude of movements. Oecologia 76:390–398. doi:10.1007/BF00377034

    Google Scholar 

  • Sinsch U (1997) Postmetamorphic dispersal and recruitment of first breeders in a Bufo calamita metapopulation. Oecologia 112:42–47. doi:10.1007/s004420050281

    Article  Google Scholar 

  • Sjögren-Gulve P (1998) Spatial movement patterns in frogs: target-oriented dispersal in the pool frog, Rana lessonae. Ecoscience 5:31–38

    Google Scholar 

  • Sullivan BK, Heatwole H (Eds) (1995) Social behaviour (Amphibian biology, vol. 2). Surrey Beatty, Chipping Norton

  • Summers K, Weigt LA, Boag PT, Bermingham E (1999) The evolution of female parental care in poison frogs of the genus Dendrobates: evidence from mitochondrial DNA sequences. Herpetologica 55:254–270

    Google Scholar 

  • Switzer PV (1993) Site fidelity in predictable and unpredictable habitats. Evol Ecol 7:533–555. doi:10.1007/BF01237820

    Article  Google Scholar 

  • Switzer PV (1997) Past reproductive success affects future habitat selection. Behav Ecol Sociobiol 40:307–312. doi:10.1007/s002650050346

    Article  Google Scholar 

  • Sztatecsny M, Schabetsberger R (2005) Into thin air: vertical migration, body condition, and quality of terrestrial habitats of alpine common toads, Bufo bufo. Can J Zool 83:788–796. doi:10.1139/Z05-071

    Article  Google Scholar 

  • Taylor DH, Ferguson DE (1970) Extraoptic celestial orientation in the southern cricket frog Acris gryllus. Science 168:390–392. doi:10.1126/science.168.3929.39

    Article  PubMed  CAS  Google Scholar 

  • Toft CA (1980) Feeding ecology of thirteen syntopic species of anurans in a seasonal tropical environment. Oecologia 45:131–141. doi:10.1007/BF00346717

    Article  Google Scholar 

  • Ursprung E, Ringler M, Hödl W (2009) Phonotactic approach pattern in the dendrobatid frog Allobates femoralis (Dendrobatidae)—a spatial and temporal analysis. Behaviour 146:153–170. doi:10.1163/156853909x410711

    Article  Google Scholar 

  • Valone TJ (2007) From eavesdropping on performance to copying the behavior of others, a review of public information use. Behav Ecol Sociobiol 62:1–14. doi:10.1007/s00265-007-0439-6

    Article  Google Scholar 

  • van Wijngaarden R, van Gool S (1994) Site fidelity and territoriality in the dendrobatid frog Dendrobates granuliferus. Amphib–Reptil 15:171–181. doi:10.1163/156853894X00272

    Google Scholar 

  • Vieites DR, Rabemananjara FEC, Bora P, Razafimahatratra B, Ravoahangimalala OR, Vences M (2005) Distribution and population density of the black-eared Malagasy poison frog, Mantella milotympanum Staniszewski, 1996 (Amphibia: Mantellidae). In: Huber BA, Sinclair BJ, Lampe K (eds) African biodiversity. Molecules, organisms, ecosystems. Springer, New York, pp 197–204

    Google Scholar 

  • Wells KD (1977) The social behaviour of anuran amphibians. Anim Behav 25:666–693

    Article  Google Scholar 

  • Wells KD (2001) The energetics of calling in frogs. In: Ryan MJ (ed) Anuran communication. Smithsonian Institution, Washington, DC, pp 45–60

    Google Scholar 

  • Wells KD (2007) The ecology and behavior of amphibians. The University of Chicago Press, Chicago

    Google Scholar 

  • Wells KD, Schwartz JJ (1982) The effect of vegetation on the propagation of calls in the neotropical frog Centrolenella fleischmanni. Herpetologica 38:449–455

    Google Scholar 

  • Wells KD, Taigen TL (1986) The effect of social interactions on calling energetics in the gray treefrog (Hyla versicolor). Behav Ecol Sociobiol 19:9–18. doi:10.1007/BF00303837

    Article  Google Scholar 

  • Weygold P (1980) Zur Fortpflanzungsbiologie von Phyllobates femoralis (Boulenger) im Terrarium. Salamandra 16:215–226

    Google Scholar 

  • Weygold P (1987) Evolution of parental care in dart poison frogs (Amphibia: Anura: Dendrobatidae). Z Zoolog Syst Evol Forsch 25:51–67

    Google Scholar 

  • Wilczynski W, Brenowitz EA (1988) Acoustic cues mediate inter-male spacing in a neotropical frog. Anim Behav 36:1054–1063. doi:10.1016/S0003-3472(88) 80065-4

    Article  Google Scholar 

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Acknowledgements

We want to dedicate this work to Domingo Ribamar da Silva and Andoe Saaki “Capi” who were murdered in the camp Arataï 2 weeks after we left in 2006 (Butler 2006). Fieldwork in 2006 was funded by the University of Vienna (“Kurzfristige wissenschaftliche Arbeiten im Ausland” and “Förderstipendium”) and the Lower Austrian State Academy (“Top-Stipendium”). Fieldwork in 2005, 2007 and 2008 was supported through Austrian Science Fund grants FWF-15345 and FWF-18811 (PI Walter Hödl). We are grateful for field assistance by Julia Felling, Philippe Gaucher, Gilles Peroz and Birgit Samhaber. Permissions and logistic help in French Guiana were provided by the CNRS and the “Association Arataï”, notably Pierre Charles-Dominique, Philippe Gaucher, Muriel Nugent, Helene Richard and Alexis Domput. Fieldwork was conducted in compliance with current French and EU law.

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Ringler, M., Ursprung, E. & Hödl, W. Site fidelity and patterns of short- and long-term movement in the brilliant-thighed poison frog Allobates femoralis (Aromobatidae). Behav Ecol Sociobiol 63, 1281–1293 (2009). https://doi.org/10.1007/s00265-009-0793-7

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