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Effects of prey size and foraging mode on the ontogenetic change in feeding niche ofColostethus stepheni (Anura: Dendrobatidae)

Oecologia volume 95, pages 93–102 (1993)Cite this article

Abstract

The feeding niche ofColostethus stepheni changes during ontogeny. Small individuals eat small arthropods, principally mites and collembolans, and larger frogs eat bigger prey of other types. The shift in prey types is not a passive effect of selection for bigger prey. There is a strong relationship between electivity for prey types and frog size, independent of electivity for prey size. Four indices of general activity during foraging (number of movements, velocity, total area utilized and time spent moving), which are associated with electivity for prey types in adult frogs and lizards, did not predict the ontogenetic change in the diet ofC. stepheni. Apparently, the behavioral changes that cause the ontogenetic change inC. stepheni are more subtle than shifts in general activity during foraging. Studies of niche partitioning in communities of anurans that do not take into consideration ontogenetic changes in diet and seasonal changes in the size structures of populations present a partial and possibly erroneous picture of the potential interactions among species.

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References

  • Allmon WD (1991) A plot study of florest floor litter frogs, Central Amazon, Brazil. J Trop Ecol 7:503–522

    Google Scholar 

  • Christian KA (1982) Change in the food niche during postmetamorphic ontogeny of the frogPseudacris triseriata. Copeia 1982:73–80

    Google Scholar 

  • Clark DB, Gibbons JW (1969) Dietary shifts in the turtlePseudemys scripta (Schoepff) from youth to maturity. Copeia 1969:704–6

    Google Scholar 

  • Domínguez JF, Salvador A (1990) Disponibilidad y uso de recursos tróficos porLacerta schreiberi yPodarcis bocagei en simpatria en una localidad de la Cordillera Cantábrica, España. Amphibia-Reptilia 11:237–246

    Google Scholar 

  • Donnelly MA (1991) Feeding patterns of the strawberry poison frog,Dendrobates pumilio (Anura: Dendrobatidae). Copeia 1991:723–730

    Google Scholar 

  • Griffiths D (1975) Prey availability and the food of predators. Ecology 56:1209–1214

    Google Scholar 

  • Grossman GD (1980) Ecological aspects of ontogenetic shifts in prey size utilization in the bay goby (Pisces: Gobiidae). Oecologia 47:233–238

    Google Scholar 

  • Guillaumet JL (1987) Some structural and floristic aspects of the forest. Experientia 43:241–251

    Google Scholar 

  • Huey RB, Pianka ER (1981) Ecological consequences of foraging mode. Ecology 64:991–999

    Google Scholar 

  • Jacobs J (1974) Quantitative measurement of food selection: A modification of the forage ratio and Ivlev's electivity index. Oecologia 14:413–417

    Google Scholar 

  • Junca FA (1989) Biologia reprodutiva deColostethus marchesianus eColostethus sp. (Amphibia: Anura: Dendrobatidae). In: Christoffersen ML, Amorim DS (eds). Resumos XVI Congresso Brasileiro de Zoologia. João Pessoa, Paraiba, p 64

  • Labanick GM (1976) Prey availability, consumption and selection in the cricket frog,Acris crepitans (Amphibia, Anura: Hylidae). J Herpetol 10:293–298

    Google Scholar 

  • Lieberman SS (1986) Ecology of the leaf litter herpetofauna of a Neotropical rain forest: La Selva, Costa Rica. Acta Zool Mex 15:1–72

    Google Scholar 

  • Magnusson WE, Paiva LJ, Rocha RM, Francke CR, Kasper LA, Lima AP (1985) The correlates of foraging mode in a community of Brazilian lizards. Herpetologica 4:324–332

    Google Scholar 

  • Martins M (1989) Nova espécie deColostethus da Amazônia Central (Amphibia: Dendrobatidae). Rev Bras Biol 49:1009–1012

    Google Scholar 

  • Moreira G, Lima AP (1991) Seasonal patterns of juvenile recruitment and reproduction in four species of leaf litter frogs in central Amazonia. Herpetologica 47:295–300

    Google Scholar 

  • Mushinsky HR, Herbrard JJ, Vodopich DS (1982) Ontogeny of water snake foraging ecology. Ecology 63:1624–1629

    Google Scholar 

  • Ovaska K (1991) Diet of the frogEleutherodactylus johnstoni (Leptodactylidae) in Barbados, West Indies. J Herpetol 25:486–488

    Google Scholar 

  • Pengilley RK (1971) The food of some Australian anurans (Amphibia). J Zool London 163:93–103

    Google Scholar 

  • Perry G, Lampl I, Lerner A, Rothenstein D, Shani E, Sivan N, Werner L (1990) Foraging mode in lacertid lizards: variation and correlates. Amphibia-Reptilia 11:373–384

    Google Scholar 

  • Pianka ER (1983) Evolutionary ecology, 3rd edn. Harper and Row, New York

    Google Scholar 

  • Pough FH, Taigen TL (1990) Metabolic correlates of foraging and social behavior of dart-poison frogs. Anim Behav 39:145–155

    Google Scholar 

  • Pough FH, Heiser JB, McFarland WN (1989) Vertebrate life, 3rd edn. Macmillan Publishing Company, New York

    Google Scholar 

  • Rose BR (1976) Habitat and prey selection ofSceloporus occidentalis andSceloporus graciosus. Ecology 57:531–541

    Google Scholar 

  • Ross ST (1978) Trophic ontogeny of the leopard sea robin,Prinotus scitulus (Pisces: Triglidae). Fish Bull 76:225–234

    Google Scholar 

  • Schoener TW (1979) Generality of the size-distance relation in models of optimal foraging. Am Nat 114:902–914

    Google Scholar 

  • Schoener TW, Gorman GC (1968) Some niche differences in three Lesser Antillean lizards of the genusAnolis. Ecology 49:819–830

    Google Scholar 

  • Schoener TW, Janzen D (1968) Notes on environmental determinants of tropical versus temperate insect size patterns. Am Nat 102:207–224

    Google Scholar 

  • Simon MP, Toft CA (1991) Diet specialization in small vertebrates: mite-eating in frogs. Oikos 61:263–278

    Google Scholar 

  • Stoner AW, Livingstone RJ (1984) Ontogenetic patterns in diet and feeding morphology in sympatric sparid fishes from seagrass meadows. Copeia 1984:174–187

    Google Scholar 

  • Strüssmann C, Ribeiro do Vale MB, Meneghini MH, Magnusson WE (1984) Diet and foraging mode ofBufo marinus and Leptodactylusocellatus. J Herpetol 18:138–146

    Google Scholar 

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

    Google Scholar 

  • Toft CA (1981) Feeding ecology of Panamanian litter anurans: Patterns in diet and foraging mode. J Herpetol 15:139–144

    Google Scholar 

  • Toft CA (1982) Community structure of litter anurans in a tropical forest Makokou, Gabon: A preliminary analysis in the minor dry season. Rev Ecol Terre Vie 36:224–232

    Google Scholar 

  • Toft CA (1985) Resource partitioning in amphibians and reptiles. Copeia 1985: 1–20

    Google Scholar 

  • Werner EE, Gilliam JF (1984) The ontogenetic niche and species interactions in size-structured populations. Annu Rev Ecol Syst 15:393–425

    Google Scholar 

  • Wiggins DA (1992) Foraging success of leopard frogs (Rana pipiens). J Herpetol 26:87–88

    Google Scholar 

  • Wilkinson L (1990) SYSTAT: The system of statistics. SYSTAT, Evanston, Illinois

    Google Scholar 

  • Woolbright LL, Stewart MM (1987) Foraging success of the tropical frog,Eleutherodactylys coqui: The cost of calling. Copeia 1987:69–75

    Google Scholar 

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Authors and Affiliations

  1. Dept. de Ecologia, INPA, CP 478, 69011-970, Manaus, AM, Brasil

    Albertina P. Lima & Gloria Moreira

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  1. Albertina P. Lima
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  2. Gloria Moreira
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Lima, A.P., Moreira, G. Effects of prey size and foraging mode on the ontogenetic change in feeding niche ofColostethus stepheni (Anura: Dendrobatidae). Oecologia 95, 93–102 (1993). https://doi.org/10.1007/BF00649512

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  • DOI: https://doi.org/10.1007/BF00649512

Key words

  • Ontogenetic change
  • Diet
  • Electivity
  • Prey size
  • Foraging behavior