Skip to main content
Log in

Endozoochory by an ilyophagous fish in the Paraná River floodplain: a window for zooplankton dispersal

  • Primary Research Paper
  • Published:
Hydrobiologia Aims and scope Submit manuscript

Abstract

Fish can have an important role in the passive dispersal of freshwater zooplankton. In the Paraná River system the migratory fish Prochilodus lineatus (Valenciennes) constitutes about 60% of the fish biomass, the adult individuals have an ilyophagous feeding mode adapted to feed on soft bottom sediments. We hypothesize that P. lineatus ingests resting stages of zooplankton along with bottom sediments and that these resting stages are able to hatch after passing through the digestive tract. Forty adult P. lineatus individuals were caught in a lake located in the floodplain of Middle Parana River. Content of the last part of intestine was removed and divided into two equal portions and stored (3 months) at 4°C and at room temperature. Later, both portions were incubated for 27 weeks at 25°C. Hatching was controlled at 4-day intervals during the first 9 weeks of the experiment and later less frequently. At the end of the experiment, 8016 individuals were recorded, belonging to 18, mostly littoral species (15 rotifers, 2 cladocerans, and one copepod). Incubation preceded by a cooling period resulted in hatching of more species and individuals. Our results show that migratory fish may be an important vector for zooplankton dispersal.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5

Similar content being viewed by others

References

  • Alekseev, V. R., 2002. Copepoda. In Fernando, C. H. (Ed.), A Guide to Tropical Freshwater Zooplankton. Backhuys Publishers, Leiden: 123–188.

    Google Scholar 

  • Allen, M. R., 2010. Genetic and environmental factors influence survival and hatching of diapausing eggs. Limnology and Oceanography 55: 549–559.

    Article  Google Scholar 

  • Angelescu, V. & F. S. Gneri, 1949. Adaptaciones del aparato digestivo al régimen alimenticio de algunos peces del rio Uruguay y rio de La Plata. Tipo omnívoro e iliófago en representantes de las familias “Loricaridae” y “Anostomatidae”. Revista Ciencias Zoológicas 1: 162–214.

    Google Scholar 

  • Battauz, Y. S., S. B. José de Paggi & J. C. Paggi, 2014. Passive zooplankton community in dry littoral sediment: reservoir of diversity and potential source of dispersal in a subtropical floodplain lake of the Middle Paraná River (Santa Fe, Argentina). International Review of Hydrobiology 99: 277–286.

    Article  Google Scholar 

  • Battistoni, P., 1995. Copepoda. In Lopretto, E. & G. Tell (eds), Ecosistemas de aguas continentales. Metodologías para su estudio. Ediciones Sur, La Plata: 953–971.

    Google Scholar 

  • Bayo, V. & E. Cordiviola de Yuan, 1996. Food assimilation of a neotropical riverine detritivorous fish, Prochilodus lineatus, studied by fatty acid composition (Pisces, Curimatidae). Hydrobiologia 330: 81–88.

    Article  CAS  Google Scholar 

  • Bilton, D. T., J. R. Freeland & B. Okamura, 2001. Dispersal in freshwater invertebrates. Annual Review of Ecology and Systematics 32: 159–181.

    Article  Google Scholar 

  • Bonetto, A. & H. P. Castello, 1985. Pesca y piscicultura en aguas continentales de América Latina. OEA, Washington.

    Google Scholar 

  • Bonetto, A. A., E. Cordiviola de Yuan, C. Pignalberi & O. Oliveros, 1969. Ciclos hidrológicos del río Paraná y las poblaciones de peces contenidas en las cuencas temporarias de su valle de inundación. Physis 29: 213–223.

    Google Scholar 

  • Bonetto, A. A., M. Canon Veron & D. Roldan, 1981. Nuevos aportes al conocimiento de las migraciones de peces en el río Paraná. Ecosur 8: 29–40.

    Google Scholar 

  • Bonetto, A. A., I. Waiss & H. Castello, 1989. The increasing damming of the Paraná basin and its effects on the lower reaches. Regulated Rivers 4: 333–346.

    Article  Google Scholar 

  • Botsford, L. W., J. W. White, M. A. Coffroth, C. B. Paris, S. Planes, T. L. Shearer, S. R. Thorrold & G. P. Jones, 2009. Connectivity and resilience of coral reef metapopulations in marine protected areas: matching empirical efforts to predictive needs. Coral Reefs 28: 327–337.

    Article  PubMed Central  PubMed  Google Scholar 

  • Bowen, S. H., 1983. Detritivory in neotropical fish communities. Environmental Biology of Fishes 9: 137–144.

    Article  Google Scholar 

  • Brendonck, L. & L. De Meester, 2003. Egg banks in freshwater zooplankton: evolutionary and ecological archives in the sediment. Hydrobiologia 491: 65–84.

    Article  Google Scholar 

  • Cáceres, C. E. & D. A. Soluk, 2002. Blowing in the wind: a field test of overland dispersal and colonization by aquatic invertebrates. Oecologia 131: 402–408.

    Article  Google Scholar 

  • Chittapun, S., P. Pholpunthin & H. Segers, 2005. Restoration of tropical peat swamp rotifer communities after perturbation: an experimental study of recovery of rotifers from the resting egg bank. Hydrobiologia 546: 281–289.

    Article  Google Scholar 

  • Clarke, K. R. & R. M. Warwick, 1994. Changes in Marine Communities: An Approach to Statistical Analysis and Interpretation. PRIMER-E, Plymouth.

    Google Scholar 

  • Cook, C. D. K., 1988. Dispersion in aquatic and amphibious vascular plants. In Crawford, R. M. M. (Ed.), Plant Life in Aquatic and Amphibious Habitats. Blackwell Scientific Publications, Oxford: 179–190.

    Google Scholar 

  • Correa, S. B., K. O. Winemiller, H. Lopez-Fernandez & M. Galett, 2007. Evolutionary perspectives on seed consumption and dispersal by fishes. Bio Science 57: 748–756.

    Google Scholar 

  • Del Barco, D., D. Demonte, R. P. Sánchez & A. Espinach Ros, 2007. Antecedentes. In Espinach Ros, A. & R. P. Sanchez (eds), Proyecto de Evaluación del Recurso Sábalo en el Paraná. Informe de los resultados de la primera etapa 2005–2006 y medidas de manejo recomendadas. Serie Pesca y Acuicultura: Estudios e investigaciones aplicadas Buenos Aires. SAGPyA, Buenos Aires: 15–18.

  • Duffy, M. A., L. J. Perry, C. A. Kearns, L. J. Weider & N. G. Hairston, 2000. Paleogenetic evidence for a past invasion of Onondaga Lake, New York, by exotic Daphnia curvirostris using mtDNA from dormant eggs. Limnology and Oceanography 45: 1409–1414.

    Article  Google Scholar 

  • Edmondson, W. T., 1965. Reproductive rate of planktonic rotifers as related to food and temperature. Ecological Monographs 35: 61–111.

    Article  Google Scholar 

  • Espinach Ros, A. & C. M. Fuentes, 2000. Recursos pesqueros y pesquerías de la cuenca del plata. In Bezzi, S., R. Akselman & E. Boschi (eds), Sintesis del estado de las pesquerías marítimas Argentinas y de la Cuenca del Plata). Instituto Nacional de investigación y Desarrollo Pesquero, Mar del Plata: 353–388.

    Google Scholar 

  • Frank, K. & C. Wissel, 1998. Spatial aspects of metapopulation survival – from model results to rules of thumb for landscape management. Landscape Ecology 13: 363–379.

    Article  Google Scholar 

  • Garcia-Roger, E. M., X. Armengol, M. J. Carmona & M. Serra, 2008. Assessing rotifer diapausing egg bank diversity and abundance in brackish temporary environments: an ex situ sediment incubation approach. Fundamental and Applied Limnology 173: 79–88.

    Article  Google Scholar 

  • Gyllström, M. & L. A. Hansson, 2004. Dormancy in freshwater zooplankton: induction, termination and the importance of benthic-pelagic coupling. Aquatic Science 66: 274–295.

    Article  Google Scholar 

  • Hairston, N. G., M. Kearns & D. R. Engstrom, 1995. Age and survivorship of diapausing eggs in a sediment egg bank. Ecology 76: 1706–1711.

    Article  Google Scholar 

  • Hammer, Ø., D. A. T. Harper & P.D. Ryan, 2001. PAST: paleontological statistics software package for education and data analysis. Palaeontologia [available on internet at http://www.palaeo-electronica.org/2001_1/past/past.pdf].

  • Harrison, S. & A. D. Taylor, 1997. Empirical evidence for metapopulation dynamics. In Hanski, I. A. & M. E. Gilpin (eds), Metapopulation Biology. Academic Press, San Diego, CA: 27–42.

    Chapter  Google Scholar 

  • Havel, J. E. & J. B. Shurin, 2004. Mechanisms, effects, and scales of dispersal in freshwater zooplankton. Limnology and Oceanography 49: 1229–1238.

    Article  Google Scholar 

  • Hutchinson, G. E., 1967. A Treatise on Limnology. I. Introduction to Lake Biology and Limnoplankton. Wiley, New York.

    Google Scholar 

  • Iriondo, M., 1993. Geomorphology and late quaternary of the Chaco (South America). Geomorphology 7: 289–303.

    Article  Google Scholar 

  • Jarnagin, S. T., B. K. Swan & W. C. Kerfoot, 2000. Fish as vectors in the dispersal of Bythotrephes cederstroemi: diapausing eggs survive passage through the gut. Freshwater Biology 43: 579–589.

    Article  Google Scholar 

  • Jarnagin, S. T., W. C. Kerfoot & B. K. Swan, 2004. Zooplankton life cycles: direct documentation of pelagic births and deaths relative to diapausing egg production. Limnology and Oceanography 49: 1317–1332.

    Article  Google Scholar 

  • Jenkins, D. G. & M. O. Underwood, 1998. Zooplankton may not disperse readily in wind, rain, or waterfowl. Hydrobiology 387: 15–21.

    Article  Google Scholar 

  • Junk, W. J., P. B. Bayley & R. E. Sparks, 1989. The flood pulse concept in river floodplain systems. Canadian Special Publication of Fisheries and Aquatic Sciences 106: 110–127.

    Google Scholar 

  • Kořínek, V., 2002. Cladocera. In Fernando, C. H. (Ed.), A Guide to Tropical Freshwater Zooplankton. Backhuys Publishers, Leiden: 69–122.

    Google Scholar 

  • Korovchinsky, N. M., 1992. Sididae and Holopediidae (Crustacea: Daphniiformes). Guides to the Identification of the Microinvertebrates of the Continental Waters of the World, Vol. III. SPB Academic Publishing, Amsterdam.

    Google Scholar 

  • Koste, W., 1978. Die Rädertiere Mitteleuropas. Borntraeger, Berlin.

    Google Scholar 

  • Leccia, M. F., 1972. Consideraciones sobre la sistemática de la familia Prochilodontidae (Osteichthyes, Cypriniformes), con una sinopsis de las especies de Venezuela. Acta Biologica Venezuelica 8: 35–96.

    Google Scholar 

  • Leibold, M. A., M. Holyoak, J. M. Chase, M. F. Hoopes, R. D. Holt, J. B. Shurin, R. Law, D. Tilman, M. Loreau & A. Gonzalez, 2004. The metacommunity concept: a framework for multi-scale community ecology. Ecology Letters 7: 601–613.

    Article  Google Scholar 

  • Magurran, A., 1988. Ecological Biodiversity and its Measurement. Princeton University Press, New York.

    Book  Google Scholar 

  • Maia-Barbosa, P. M., E. M. Eskinazi-Santanna, C. F. Valadares & G. C. D. Pessoa, 2003. The resting eggs of zooplankton from a tropical, eutrophic reservoir (Pampulha Reservoir, south-east Brazil). Lakes & Reservoirs: Research & Management 8: 269–275.

    Article  Google Scholar 

  • Mellors, W. K., 1975. Selective predation of ephippial Daphnia and the resistance of ephippial eggs to digestion. Ecology 56: 974–980.

    Article  Google Scholar 

  • Montoya, D., M. A. Zavala, M. A. Rodríguez & D. W. Purves, 2008. Animal versus wind dispersal and the robustness of tree species to deforestation. Science 320: 1502–1504.

    Article  CAS  PubMed  Google Scholar 

  • Paggi, J. C., 2004. Importancia de la fauna de “Cladóceros” (Crustacea, Branchiopoda) del Litoral Fluvial Argentino. INSUGEO Miscelanea 12: 239–246.

    Google Scholar 

  • Palazzo, F., C. Costa Bonecker & A. P. C. Fernandez, 2008. Resting cladoceran eggs and their contribution to zooplankton diversity in a lagoon of the Upper Paraná River floodplain. Lakes & Reservoirs: Research & Management 13: 207–214.

    Article  Google Scholar 

  • Pollux, B. J. A., 2011. The experimental study of seed dispersal by fish (Ichthyochory). Freshwater Biology 56: 197–212.

    Article  Google Scholar 

  • Proctor, V. W., 1964. Viability of crustacean eggs removed from ducks. Ecology 45: 656–658.

    Article  Google Scholar 

  • Proctor, V. W., C. R. Malone & V. L. De Vlaming, 1967. Dispersal of aquatic organisms: viability of disseminules recovered from the intestinal tracts of captive Killdeer. Ecology 48: 672–676.

    Article  Google Scholar 

  • Rossi, L. M., 1992. Evolución morfológica del aparato digestivo de postlarvas y prejuveniles de Prochilodus lineatus (Val., 1847) (Pisces, Curimatidae) y su relación con la dieta. Revista Hidrobiologia Tropical 25: 159–167.

    Google Scholar 

  • Santangelo, J. M., L. Rabelo Araújo, F. A. Esteves & M. Manca, 2011. Method for hatching resting eggs from tropical zooplankton: effects of drying or exposing to low temperatures before incubation. Acta Limnologica Brasiliensia 23: 42–47.

    Article  Google Scholar 

  • Segers, H., 1995. Rotifera. In Dumont, H. J. (Ed.), Guides to the Identification of the Microinvertebrates of the Continental Waters of the World. Backhuys Publishers, Leiden: 1–226.

    Google Scholar 

  • Segers, H. & D. Smet, 2008. Diversity and endemism in Rotifera: a review, and Keratella Bory de St Vincent. Biodiversity & Conservation 17: 303–316.

    Article  Google Scholar 

  • Simberloff, D. & M. Rejmanek (eds), 2010. Encyclopedia of Biological Invasions. University of California Press, Berkeley.

    Google Scholar 

  • Sørensen, T. A., 1948. Method of establishing groups of equal amplitude in plant sociology based on similarity of species content and its application to analyses of vegetation on Danish commons. Videnski Selskab Biologiske Skrifter 5: 1–34.

    Google Scholar 

  • Shiel, R. J., K. F. Walker & W. D. Williams, 1982. Plankton of the lower River Murray South Australia. Australian Journal of Marine & Freshwater Research 33: 301–327.

    Article  Google Scholar 

  • Shurin, J. B. & J. E. Havel, 2003. Hydrologic connections as dispersal roues for the spread of the exotic cladoceran Daphnia lumholtzi. Biological Invasions 4: 431–439.

  • Tablado, A. & N. Oldani, 1984. Consideraciones generales sobre las migraciones de peces en el río Paraná. Boletín de la Asociación de Ciencias Naturales del Litoral 4: 31–34.

    Google Scholar 

  • Torres, R. & E. Zoppi de Roa, 2010. Latencia en cladóceros y copépodos (Crustacea) de un humedal de la península de Paria, Venezuela. Metodos en Ecologia y Sistematica 5: 23–35.

    Google Scholar 

  • Vandekerkhove, J., B. Niessen, S. Declerck, E. Jeppesen, J. M. C. Conde-Porcuna, L. Brendonck & L. De meester, 2004. Hatching rate and hatching success with and without isolation of zooplankton resting stages. Hydrobiologia 526: 235–241.

    Article  Google Scholar 

  • Vandekerkhove, J., S. Declerck, L. Brendonck, J. M. C. Conde-Porcuna, E. Jeppesen, L. S. Johansson & L. De meester, 2005. Uncovering hidden species: hatching diapausing eggs for the analysis of cladoceran species richness. Limnology and Oceanography Methods 3: 399–407.

    Article  Google Scholar 

  • Wilson, D. S., 1992. Complex interactions in metacommunities, with implications for biodiversity and higher levels of selection. Ecology 73: 1984–2000.

    Article  Google Scholar 

Download references

Acknowledgments

This research was funded by Provincia de Santa Fe (SECTeI 2010-037-11). We thank Lic. Danilo Demonte and Dr. Pablo Scarabotti for their generous assistance to the collection of fish samples.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Yamila S. Battauz.

Additional information

Handling editor: Mariana Meerhoff

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Battauz, Y.S., de Paggi, S.B.J. & Paggi, J.C. Endozoochory by an ilyophagous fish in the Paraná River floodplain: a window for zooplankton dispersal. Hydrobiologia 755, 161–171 (2015). https://doi.org/10.1007/s10750-015-2230-4

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10750-015-2230-4

Keywords

Navigation