Skip to main content

Advertisement

Log in

Community structure of the macroinfauna inhabiting tidal flats characterized by the presence of different species of burrowing bivalves in Southern Chile

  • Biodiversity in Enclosed Seas
  • Published:
Hydrobiologia Aims and scope Submit manuscript

Abstract

Several species of bivalves coexist at the lower intertidal of large tidal flats located in the enclosed or inland coast of the northern area of the Nord-Patagonic archipelagos on the Chilean coast (ca. 40–42°S): Tagelus dombeii (Lamarck), Mulinia edulis (King & Broderip), Venus antiqua King & Broderip, Semele solida (Gray), Gari solida (Gray) and Diplodonta insconspicua Philippi. To explore possible spatial variation in the community structure of the macroinfauna inhabiting sediments with different assemblages of these bivalves, seasonal sampling was carried out during 2003–2004 at two tidal flats of that area. Higher species richness and specimen densities of the macroinfauna occurred in sediments with the higher densities of bivalves, especially in sediments where the deep burrower T. dombeii reaches its greatest abundances. Our results suggest that, apart from presence of bivalves, the burrowing depth of these organisms is also important in promoting the abundance of macroinfauna. Our results are in contrast with earlier conceptualizations for community organization of the soft bottom macroinfauna inhabiting intertidal flats, related to biological interactions occurring among different phyletic groups, such as that arguing that suspension feeding bivalves (such as T. dombeii and V. antiqua) will negatively affect the recruitment of species with planktonic larvae, by filtering them before they become established in the substrate. Thus, it is concluded that beneficial effects of bivalve bioturbation overcome that negative effects on the macroinfauna, although detrimental effects may well occur at bivalve densities higher than those studied here.

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
Fig. 6

Similar content being viewed by others

References

  • Anderson, F., L. Black, L. Mayer & L. Watling, 1981. A temporal and spatial study of a mud flat texture. Northeastern Geology 3: 184–196.

    Google Scholar 

  • Black, L. F., 1980. The biodeposition cycle of a surface deposit-feeding bivalve, Macoma balthica (l.). In Kennedy V. S. (ed) Estuarine Perspectives. Academic Press, New York: 389–402.

    Google Scholar 

  • Carr, M. R., 1997. PRIMER User Manual. Plymouth Marine Laboratory, Prospect Place, Plymouth PL1 3 DH, United Kingdom, 40 pp.

  • Clarke, K. R., 1993. Non-parametric multivariate analyses of changes in community structure. Australian Journal of Ecology 18: 117–143.

    Article  Google Scholar 

  • Commito, J. A., 1987. Adult–larval interactions: predictions, mussels and cocoons. Estuarine Coastal and Shelf Science 25: 599–606.

    Article  Google Scholar 

  • Commito, J. A. & N. M. J. A. Dankers, 2001. Dynamics of spatial and temporal complexity in European and North American soft-bottom mussel beds. In: Reise, K. (ed.), Ecological Comparisons of Sedimentary Shores. Ecological Studies 151: 39–59.

  • Commito, J. A., E. A. Celano, H. J. Celico, S. Como & C. P. Johnson, 2005. Mussels matter: postlarval dispersal dynamics altered by a spatially complex ecosystem engineer. Journal of Experimental Marine Biology and Ecology 316: 133–147.

    Article  Google Scholar 

  • Dame, R. F., 1996. Ecology of Marine Bivalves: an ecosystem approach. CRC Press, New York.

    Google Scholar 

  • Dame R. F., D. Bushek & T. C. Prins, 2001. Benthic suspension feeders as determinants of ecosystem structure and function in shallow coastal waters. In Reise, K. (ed.), Ecological Comparisons of Sedimentary Shores. Ecological Studies 151: 11–37.

  • Dittmann, S., 1990. Mussel beds – amensalism or amelioration for intertidal fauna ? Helgoländer Meeresuntersuchungen 44: 335–352.

    Article  Google Scholar 

  • Emery, K. O., 1938. A simple method of mechanical analysis of sands. Journal of Sedimentary Petrology 8: 105–111.

    Google Scholar 

  • Gutiérrez, D., V. A. Gallardo, S. Mayor, C. Neira, C. Vásquez, J. Sellanes, M. Rivas, A. Soto, F. Carrasco & M. Baltazar, 2000. Effects of dissolved oxygen and fresh organic matter on the bioturbation potential of macrofauna in sublittoral sediments off Central Chile during the 1997/1998 El Niño. Marine Ecology Progress Series 202: 81–99.

    Google Scholar 

  • Hall, S. J., 1994. Physical disturbance and marine benthic communities: life in unconsolidated sediments. Oceanography and Marine Biology: an annual review 32: 179–239.

    Google Scholar 

  • Kanaya, G., E. Nobata, T. Toya & E. Kikuchi, 2005. Effects of different feeding habits of three bivalve species on sediment characteristics and benthic diatom abundance. Marine Ecology Progress Series 299: 67–78.

    Google Scholar 

  • Lardies, M. A., E. Clasing, J. M. Navarro & R. A. Stead, 2001. Effects of environmental variables on burial depth of two infaunal bivalves inhabiting a tidal flat in southern Chile. Journal of the Marine Biological Association of the U.K. 81: 809–816.

    Article  Google Scholar 

  • Legendre, P., S. F. Thrush, V. J. Cummings, P. K. Dayton, J. Grant, J. E. Hewitt, A. H. Hines, B. H. McArdle, R. D. Pridmore, D. C. Schneider, S. J. Turner, R. B. Whitlatch & M. R. Wilkinson, 1997. Spatial structure of bivalves in a sandflat: scale and generating processes. Journal of Experimental Marine Biology and Ecology 216: 99–128.

    Article  Google Scholar 

  • Michaud, E., G. Desrosiers, F. Mermillod-Blondin, B. Sundby & G. Stora, 2005. The functional group approach to bioturbation: I. The effects of biodiffusers and gallery-diffusers of the Macoma balthica community on sediment oxygen uptake. Journal of Experimental Marine Biology and Ecology 326: 77–88.

    Article  CAS  Google Scholar 

  • Michaud, E., G. Desrosiers, F. Mermillod-Blondin, B. Sundby & G. Stora, 2006. The functional group approach to bioturbation: II. The effects of the Macoma balthica community on fluxes of nutrients and dissolved organic carbon across the sediment–water interface. Journal of Experimental Marine Biology and Ecology 337: 178–189.

    Article  CAS  Google Scholar 

  • Nowell, A. R. M., P. A. Jumars & J. E. Eckman, 1981. Effects of biological activity on the entraiment of marine sediments. Marine Geology 42: 133–153.

    Article  Google Scholar 

  • Peterson, C. H., 1977. Competitive organization of the soft-bottom macrobenthic communities of Southern California Lagoons. Marine Biology 43: 343–359.

    Article  Google Scholar 

  • Ragnarsson, S. A. & D. Raffaelli, 1999. Effects of the mussel Mytilus edulis L. on the invertebrate fauna of sediments. Journal of Experimental Marine Biology and Ecology 241: 31–43.

    Article  Google Scholar 

  • Reise, K., 1983. Biotic enrichment of intertidal sediments by experimental aggregates of the deposit-feeding bivalve Macoma balthica. Marine Ecology Progress Series 12: 229–236.

    Google Scholar 

  • Rhoads, D. C. & D. K. Young, 1970. The influence of deposit-feeding organism on sediment stability and community trophic structure. Journal Marine Research 28: 150–178.

    Google Scholar 

  • Rhoads, D. C. & L. F. Boyer, 1982. The effects of marine benthos on physical properties of sediments: a successional perspective. In McCall P. L. & M. J. S. Tevesz (eds) Animal-Sediment Relations – The Biogenic Alteration of Sediments. Plenum Press, New York: 3–52.

    Google Scholar 

  • Seward-Thompson, B. & J. Hails, 1973. An appraisal on the computation of statistical parameters in grain size analysis. Sedimentology 11: 83–98.

    Google Scholar 

  • Sokal, R. R. & F. J. Rohlf, 1995. Biometry: the principles and practice of statistics in biological research. Freeman, W.H., New York, 1–877.

    Google Scholar 

  • Stead, R. A., E. Clasing, M.A. Lardies, L.P. Arratia, G. Urrutia & O. Garrido, 2002. The significance of contrasting feeding strategies on the reproductive cycle in two coexisting tellinacean bivalves. Journal of the Marine Biological Association of the U.K. 82: 443–453.

    Article  Google Scholar 

  • Vaughn, C. C. & C. C. Hakenkamp, 2001. The functional role of burrowing bivalves in freshwater ecosystems. Freshwater Biology 46: 1431–1446.

    Article  Google Scholar 

  • Vaughn, C. C. & D. E. Spooner, 2006. Unionid mussels influence macroinvertebrate assemblage structure in streams. Journal of the North American Benthological Society 25: 691–700.

    Article  Google Scholar 

  • Viviani, C. A., 1979. Ecogeografia del litoral chileno. Studies on Neotropical Fauna and Environment 14: 65–123.

    Article  Google Scholar 

  • Woodin, S. A., 1976. Adult–larval interactions in dense infaunal assemblages: Patterns of abundance. Journal of Marine Research 34: 25–41.

    Google Scholar 

Download references

Acknowledgements

To M. González for sorting faunistical samples and sedimentary analyses. To two anonymous reviewers who greatly improved an earlier manuscript. This research was supported by CONICYT, Chile (Fondecyt Project No. 1030335). Funds given to EJ to present this study during the 39th European Marine Biology Symposium (Genoa, Italia; July 2004) came from Dirección de Investigación y Desarrollo, Universidad Austral de Chile and Fondecyt Project No. 1030335.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to E. Jaramillo.

Electronic supplementary material

Below are the electronic supplementary materials.

ESM (DOC 66kb)

Rights and permissions

Reprints and permissions

About this article

Cite this article

Jaramillo, E., Contreras, H. & Duarte, C. Community structure of the macroinfauna inhabiting tidal flats characterized by the presence of different species of burrowing bivalves in Southern Chile. Hydrobiologia 580, 85–96 (2007). https://doi.org/10.1007/s10750-006-0463-y

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10750-006-0463-y

Keywords

Navigation