Environmental Biology of Fishes

, Volume 89, Issue 1, pp 11–19 | Cite as

Reproductive strategies of Red-bellied Piranha (Pygocentrus nattereri Kner, 1858) in the white waters of the Mamirauá flooded forest, central Brazilian Amazon

  • Helder Lima Queiroz
  • Marcela B. Sobanski
  • Anne E. Magurran
Article

Abstract

Despite being an important member of neotropical fish assemblages, as well as a species with an unenviable reputation, little is known about the reproductive ecology of Red-bellied Piranha, Pygocentrus nattereri, in the wild. We tracked the reproductive activity of piranhas in the flooded forests of Mamirauá Reserve, Central Brazilian Amazon, for 2 years, in an investigation that included over 3,000 individual fish. Contrary to expectation piranhas had not one, but rather two annual reproductive seasons, tuned to water level fluctuation and the flooding pulse. Females were found to have up to 30,000 oocytes, little more than one third of which were mature and available for spawning in a single batch. Sexual maturation (of both males and females) occurred at around 160 mm. At this point sexually active individuals (of both sexes) became dark and lost most of their red coloration. Ontogenetic changes in habitat selection were strongly associated with the spawning behavior of mature adults. We also found that flooded marginal vegetation and marginal grasses inside lakes were the preferred spawning areas. In contrast, non-reproductive individuals were found in open water and under floating meadows.

Keywords

Red-bellied Piranha Pygocentrus Serrasalminae Reproductive biology Life-history strategies Amazon 

References

  1. Araújo-Lima C, Goulding M (1997) So fruitful a fish: ecology, conservation, and aquaculture of the Amazon´s Tambaqui. Columbia University Press, New York, 192ppGoogle Scholar
  2. Crampton W (1999) A fauna de peixes da Reserva Mamirauá. In: Queiroz H, Crampton W (eds) O Manejo Integrado dos Recursos Pesqueiros em Mamirauá. SCM, CNPq/MCT, Brasília (DF), 205ppGoogle Scholar
  3. Duponchelle F, Lino F, Hubert N, Panfili J, Renno J-F, Baras E, Torrico JP, Dugue R, Nuñez J (2007) Environment-related life-history trait variations of the Red-bellied Piranha Pygocentrus nattereri in two river basins of the Bolivian Amazon. J Fish Biol 71:1113–1134CrossRefGoogle Scholar
  4. Ferreira RMA, Bazzoli N, Rizzo E, Sato Y (1996) Aspectos reprodutivos da piranha, Pygocentrus piraya (Teleostei, Characiformes), espécie nativa da bacia do Rio São Francisco. Arq Bras Med Vet Zootec 48(1):71–76Google Scholar
  5. Fink W (1993) Revision of the piranha genus Pygocentrus (Teleostei, Characiformes). Copeia 1993:665–687CrossRefGoogle Scholar
  6. Goulding M (1980) The fishes and the forest. Explorations in Amazonian natural history. University of California Press, Berkeley, 280pGoogle Scholar
  7. Henderson P, Crampton W (1997) A comparison of fish diversity and abundance between nutrient-rich and nutrient-poor lakes in the upper Amazon. J Trop Ecol 13:175–198CrossRefGoogle Scholar
  8. Henderson P, Hamilton HF (1995) Standing crop and distribution of fish in drifting and attached floating meadow within an upper Amazonian varzea lake. J Fish Biol 47:266–276CrossRefGoogle Scholar
  9. Henderson P, Robertson B (1997) On structural complexity and fish diversity in an Amazonian floodplain. In: Padoch C, Ayres J, Vásquez M, Henderson A (eds) Várzea: diverstity, development, and conservation of Amazonian´s whitewater floodplains. Advances in Economic Botany, vol. 13:45–58. The New York Botanical Garden Press, 407ppGoogle Scholar
  10. Hubert N, Renno JF (2006) Historical biogeography of South American freshwater fishes. J Biogeogr 33:1414–1436CrossRefGoogle Scholar
  11. Junk WJ (1997) The Central Amazon floodplain—ecology of a pulsing system. Ecological Studies, 126. Springer, Berlin, 525pGoogle Scholar
  12. Junk WJ, Ohly JJ, Piedade MTF, Soares MGM (2000) The Central Amazon floodplain: actual use and options for a sustainable management. Backhuys, Leiden, 584ppGoogle Scholar
  13. Lamas IR, Godinho AL (1996) Reproduction in the piranha Serrasalmus spiropleura, a neotropical fish with a unusual pattern of sexual maturity. Environ Biol Fish 45:161–168CrossRefGoogle Scholar
  14. Latini AO, Petrere M Jr (2004) Reduction of a native fish fauna by alien species: an example from Brazilian freshwater tropical lakes. Fisheries Manag Ecol 11:71–79CrossRefGoogle Scholar
  15. Leão ELM, Leite RG, Chaves PTC, Ferraz E (1991) Aspectos da reprodução, alimentação e parasitofauna de uma espécie rara de piranha, Serrasalmus altuvei Ramírez, 1956 (Pisces, Serrasalmidae) do baixo rio Negro. Rev Bras Biol 51:545–553Google Scholar
  16. Lowe-McConnell RH (1964) The fishes of the Rupununi Savana district of British Guyana, South America. J Linn Soc (Zool) 45:103–144CrossRefGoogle Scholar
  17. Lowe-McConnell RH (1987) Ecological studies in tropical fish communities. Cambridge University Press, CambridgeCrossRefGoogle Scholar
  18. Lowe-McConnell RH (1999) Estudos Ecológicos de Comunidades de Peixes Tropicais. Editora da Universidade de São Paulo, São Paulo, 534ppGoogle Scholar
  19. Machado-Alison A (1983) Estudios sobre la sistemática de la subfamilia Serrasalminae (Teleostei, Characidae). Parte II. Discusión sobre la condicion monofilética de la subfamilia. Acta Biol Venez 11:145–195Google Scholar
  20. Machado-Alison A, Fink W (1995) Sinopsis de las especies de la subfamilia Serrasalminae presentes en la cuenca del Orinoco. Claves, Diagnosis e Ilustraciones. Lito Color RI, CaracasGoogle Scholar
  21. Magurran AE, Queiroz HL (2003) Partner choice in piranha shoals. Behaviour 140:289–299CrossRefGoogle Scholar
  22. Pauly D (1994) Quantitative analysis of published data on the growth, metabolism, food consumption, and related features of the Red-bellied Piranha, Serrasalmus nattereri (Characidae). Environ Biol Fish 41:423–437Google Scholar
  23. Petry P, Bayley PB, Markle DF (2003) Relationships between fish assemblages, macrophytes and environmental gradients in the Amazon River floodplain. J Fish Biol 63:547–579CrossRefGoogle Scholar
  24. Quaggio-Grassiotto I, Guimarães ACD (2003) Follicular epithelium, theca and egg envelope formation in Serrasalmus spilopleura (Teleostei, Characiformes, Characidae). Acta Zool (Stockholm) 84:121–129CrossRefGoogle Scholar
  25. Queiroz HL (1997) Artisanal fisheries of pirarucu at the Mamirauá ecological station. In: Padoch C, Ayres JM, Pinedo-Vasquez M, Henderson A (eds) Várzea: diversity, development, and conservation of Amazonian´s whitewater floodplains. Advances in Economic Botany, vol.13:83–100. The New York Botanical Garden Press, 407pGoogle Scholar
  26. Queiroz HL, Crampton W (eds) (1999) O Manejo Integrado dos Recursos Pesqueiros em Mamirauá. SCM, CNPq/MCT, Brasília, 205ppGoogle Scholar
  27. Queiroz HL, Magurran AE (2005) Safety in numbers? Shoaling behaviour of the Amazonian Red-bellied Piranha. Biol Lett 1(2):155–157CrossRefPubMedGoogle Scholar
  28. Ramalho EE, Macedo J, Vieira TM, Valsecchi J, Calvimontes J, Marmontel M, Queiroz HL (2009) Ciclo hidrológico nos ambientes de várzea da Reserva de Desenvolvimento Sustentável Mamirauá—Médio Rio Solimões, Período de 1990 a 2008. Uakari 5(1):61–87Google Scholar
  29. Rodrigues JD, Mota A, Moraes MN, Ferreira AE (1978) Curvas de maturação gonadal e crescimento de fêmeas de pirambeba, Serrasalmus spiropleura Kner, 1859 (Pisces, Cypriniformes). Bol Inst Pesca 5:51–63Google Scholar
  30. Saint-Paul U, Zuanon J, Villacorta-Correa MA, Garcia M, Fabre N, Berger U, Junk WJ (2000) Fish communities in central white- and black-water floodplains. Environ Biol Fish 57:235–250CrossRefGoogle Scholar
  31. Sato Y, Sampaio EV, Fenechi-Verani N, Verani JR (2006) Biologia reprodutiva de duas espécies de Characidae (Osteichthyes, Characiformes) na Bacia do São Francisco, Minas Gerais. Brasil Rev Bras Zool 23(1):267–273Google Scholar
  32. Sazima I, Guimarães SA (1987) Scavenging on human corpses as a source for stories about man-eating piranhas. Environ Biol Fish 20:75–77CrossRefGoogle Scholar
  33. Sazima I, Machado FA (1990) Underwater observation of piranhas in western Brazil. Environ Biol Fish 28:17–31CrossRefGoogle Scholar
  34. Schulte W (1988) Piranhas in the aquarium. Tropical Fish Hobbyist Publication, Neptune CityGoogle Scholar
  35. Sioli H (ed) (1984) The Amazon: limnology and landscape ecology of a mighty tropical river and its basin. W Junk, Dordrecht, 580ppGoogle Scholar
  36. Uetanabaro M, Wang T, Abe AS (1993) Breeding behaviour of the Red-bellied Piranha Pygocentrus nattereri in nature. Environ Biol Fish 38:369–371CrossRefGoogle Scholar
  37. Vazzoler AEAM (1996) Biologia da Reprodução de Peixes Teleósteos. Teoria e Prática. Ed. EDUEM. Maringá, Paraná, 51ppGoogle Scholar
  38. Vazzoler AEAM, Menezes NA (1992) Síntese do conhecimento sobre o comportamento reprodutivo dos Characiformes da América do Sul (Teleostei, Ostariphysi). Rev Bras Biol 52:627–640Google Scholar
  39. Winemiller KO (1989) Ontogenetic diet shifts and resource partitioning among piscivorous fishes in the Venezuelan llanos. Environ Biol Fish 26:177–199CrossRefGoogle Scholar
  40. Wittmann F, Schöngart J, Montero JC, Motzer T, Junk WJ, Piedade MTF, Queiroz HL, Worbes M (2006) Tree species composition and diversity gradients in white-water forests across the Amazon Basin. J Biogeogr 33(8):1334–1347CrossRefGoogle Scholar

Copyright information

© Springer Science+Business Media B.V. 2010

Authors and Affiliations

  • Helder Lima Queiroz
    • 1
  • Marcela B. Sobanski
    • 1
  • Anne E. Magurran
    • 2
  1. 1.Mamirauá Institute for Sustainable Development—IDSM-OS/MCTTeféBrazil
  2. 2.Scottish Oceans Institute, School of BiologyUniversity of St. AndrewsSt. AndrewsUK

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