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The brackishwater hyporheic zone: invertebrate community structure across a novel ecotone

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This study describes a hyporheic zone that exists beneath a river-dominated estuary in North Wales, and which spans the freshwater/saltwater boundary. A series of 72 cores was taken from the Aber Estuary, in September, at depths from 10–60 cm below the bed surface. Site 1 was above the extreme high water mark and therefore was never inundated by salt water. Site 5 was the furthest downstream and was inundated twice daily by incoming tides. Substrates contained more gravel at the upstream sites and closer to the bed surface, with more sand and silt at downstream sites and at depth. Salinity of interstitial water increased both with distance away from Site 1 and with increasing depth into the zone, reaching a maximum of 15‰ at 60 cm at Site 5, as measured at low tide. Longitudinal and vertical zonations of the invertebrate taxa were evident, and densities were greater in the top 40 cm than below. Nematodes were especially abundant from 10–60 cm, and genera differed along the estuary. Oligochaetes were well represented at most sites, with the less saline sites yielding Naididae, Enchytraeidae, Aeolosomatidae and Tubificidae; Site 5 was dominated by Tubifex costatus. Chironomid larvae were most abundant to 40 cm at Sites 1 and 2 (primarily Brillia modesta, Corynoneura sp., Tanytarsus sp., and unidentified Tanypodinae), but they were also found at Site 3 (to 60 cm), and at 10 cm at Site 5 (Orthocladius sp.). Nymphs of mayflies and caddisfly larvae were found primarily at Site 1, but small stonefly nymphs and elmid beetle larvae were taken at Site 2 depths where the interstitial water was brackish. The most saline sediments were populated by the triclad Uteriporus vulgaris, the polychaete Nereis sp., and snails (Hydrobia sp.). Site, salinity, pH, and sand and silt contents appeared to influence species distribution most; together, these explained 37.8% of the variance (CANOCO). There was an overall negative relationship between silt content of the sediments and total invertebrate density. The hyporheic zone of the Aber Estuary is thus not only influenced by surface water and, presumably, estuarine groundwater exchanges, but is further complicated, biologically, by having a salinity gradient running through it. The term `brackishwater hyporheic zone' (BHZ) is proposed to describe this and similar systems.

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References

  • Ansari, A., C. U. Rivonkar & U. M. Sangodkar, 2001. Population fluctuation and vertical distribution of meiofauna in a tropical mudflat at Mandovi estuary, west coast of India. Indian Journal of Marine Science 30: 237-245.

    Google Scholar 

  • Bassett, D. A., 1967. A Source-Book of Geological, Geomorphological and Soil Maps for Wales and the Welsh Borders (1800-1966). Amgueddfa Genedlaethol Cymru, Cardiff. 322 pp.

  • Beukema, J. J., 1974. Seasonal changes in the biomass of the macrobenthos of tidal flat areas in the Dutch Wadden Sea. Netherlands Journal of Sea Research 8: 94-107.

    Google Scholar 

  • Boulton, A. J., P. Marmonier & J. A. Davis, 1999. Hydrological exchange and subsurface water chemistry in streams varying in salinity in south-western Australia. International Journal of Salt Lakes Research 8: 361-382.

    Google Scholar 

  • Boulton, A. J., C. Hakenkamp, M. Palmer & D. Strayer, 2002. Freshwater meiofauna and surface water-sediment linkages: a conceptual framework for cross-system comparisons. In Rundle, S. D., A. L. Robertson & J. M. Schmid-Araya (eds), Freshwater Meiofauna: Biology and Ecology. Backhuys Publishers, Leiden: 241-259.

    Google Scholar 

  • Bouwman, L. A., K. Romeyn & W. Admiraal, 1984. On the ecology of meiofauna in an organically polluted estuarine mudflat. Estuarine, Coastal and Marine Science 19: 1-17.

    Google Scholar 

  • Boyden, C. R. & C. Little, 1973. Faunal distributions in soft sediments of the Severn estuary. Estuarine, Coastal and Marine Science 1: 203-223.

    Google Scholar 

  • Brinkhurst, R. O., 1964. Observations on the biology of the marine oligochaete Tubifex costatus. Journal of the Marine Biological Association of the United Kingdom 44: 11-16.

    Google Scholar 

  • Brown, E. H., 1960. The Relief and Drainage of Wales, a Study in Geomorphological Development. University of Wales Press, Cardiff, 264 pp.

    Google Scholar 

  • Buzzelli, C. P., R. A. Luettich, S. P. Powers, C. H. Peterson, J. E. McNinch, J. L. Pinckney & H. W. Paerl, 2002. Estimating the spatial extent of bottom-water hypoxia and habitat degradation in a shallow estuary. Marine Ecology Progressive Series 230: 103- 112.

    Google Scholar 

  • Coull, B. C., 1999. Role of meiofauna in estuarine soft bottom habitats. Australian Journal of Ecology 24: 327-343.

    Google Scholar 

  • Crofton, H. D., 1966. Nematodes. Hutchinson University Library, London, 160 pp.

    Google Scholar 

  • Cummins, K. W., 1962. An evaluation of some techniques for the collection and analysis of benthic samples with special emphasis on lotic waters. American Midland Naturalist 67: 477-504.

    Google Scholar 

  • Dame, R. F. & D. M. Allen, 1996. Between estuaries and the sea. Journal of Experimental Marine Biology and Ecology 200: 169- 185.

    Google Scholar 

  • Di Sabatino, A., P. Martin, R. Gerecke & B. Cicolani, 2002. Hydrachnidia (Water Mites). In Rundle, S. D., A. L. Robertson & J. M. Schmid-Araya (eds), Freshwater Meiofauna: Biology and Ecology. Backhuys Publishers, Leiden: 105-133.

    Google Scholar 

  • Dyer, K. R., 1973. Estuaries: A Physical Introduction. John Wiley, London, 140 pp.

    Google Scholar 

  • Essink, K. & H. Keidel, 1998. Changes in estuarine nematode communities following a decrease of organic pollution. Aquatic Ecology 32: 195-202.

    Google Scholar 

  • Fraser, B. G. & D. D. Williams, 1998. Seasonal boundary dynamics of a groundwater/ surface-water ecotone. Ecology 79: 2019-2031.

    Google Scholar 

  • George, C. L. & J. A. Lindley, 1997. Hatching nauplii of planktonic calanoid copepods from intertidal estuarine sediments. Journal of the Marine Biological Association of the United Kingdom 77: 899-902.

    Google Scholar 

  • Giere, O., 1973. Oxygen in the marine hygropsammal and the vertical microdistribution of oligochaetes. Marine Biology 21: 180-189.

    Google Scholar 

  • Godbout, L. & H. B. N. Hynes, 1982. The three dimensional distribution of the fauna in a single riffle in a stream in Ontario. Hydrobiologia 97: 87-96.

    Google Scholar 

  • Goodey, T., 1963. Soil and Freshwater Nematodes (2nd ed. revised and rewritten by J. B. Goodey) Methuen, London, 544 pp.

    Google Scholar 

  • Green, J., 1968. The Biology of Estuarine Animals. Sidgwick and Jackson, London, 401 pp.

    Google Scholar 

  • Gyedu-Ababio, T. K., J. P. Furstenberg, D. Baird, & A. Vanreusel, 1999. Nematodes as indicators of pollution: a case study from the Swartkops River system, South Africa. Hydrobiologia 397: 155-169.

    Google Scholar 

  • Hakenkamp, C. C. & M. A. Palmer, 2000. The ecology of hyporheic meiofauna. In Jones, J. B. & P. J. Mulholland (eds), Streams and Ground Waters. Academic Press, Boston: 307-336.

    Google Scholar 

  • Hayashi, M. & D. O. Rosenberry, 2002. Effects of ground water exchange on the hydrology and ecology of surface water. Groundwater 40: 309-316.

    Google Scholar 

  • Hynes, H. B. N., T. T. Macan, & W. D. Williams, 1960. A key to the British species of Crustacea: Malacostraca. Freshwater Biological Association of the United Kingdom, Scientific Publication 19: 1-36.

    Google Scholar 

  • Jones, J. B. & P. J. Mulholland (eds), 2000. Streams and Ground Waters. Academic Press, Boston, 456 pp.

    Google Scholar 

  • Jones, M. B., 1972. Osmoregulation in the Jaera albifrons group of species. Journal of the Marine Biological Association of the United Kingdom 52: 419-427.

    Google Scholar 

  • Kumar, R. S., 1997. Vertical distribution and abundance of sediment-dwelling macroinvertebrates in an estuarine mangrove biotope. Indian Journal of Marine Science 26: 26-30.

    Google Scholar 

  • Li, J., M. Vincx & P. M. J. Herman, 1997. Carbon flows through meiobenthic nematodes in the Westerschelde Estuary. Fundamentals of Applied Nematology 20: 487-494.

    Google Scholar 

  • Macan, T. T., 1977. A key to the British fresh-and brackish-water gastropods. Freshwater Biological Association of the United Kingdom, Scientific Publication 13: 1-46.

    Google Scholar 

  • Mannino, A. & P. A. Montagna, 1997. Small-scale spatial variation of macrobenthic community structure. Estuaries 20: 159-173.

    Google Scholar 

  • Marshall, D. J., R. Perissinotto, C. Nozais, C-J. Haines & S. Proches, 2001. Occurrence of the astigmatid mite Tyrophagus in estuarine benthic sediments. Journal of the Marine Biological Association of the United Kingdom 81: 889-890.

    Google Scholar 

  • McLusky, D. S., 1981. The Estuarine Ecosystem. John Wiley & Sons, New York.

    Google Scholar 

  • Michaelis, H., H. Fock, M. Grotjahn & D. Post, 1992. The status of the intertidal zoobenthic brackish-water species in estuaries of the German Bight. Netherlands Journal of Sea Research 30: 201-207.

    Google Scholar 

  • Miller, D. C., S. L. Poucher & L. Coiro, 2002. Determination of lethal dissolved oxygen levels for selected marine and estuarine fishes, crustaceans, and a bivalve. Marine Biology 140: 287-296.

    Google Scholar 

  • Ndaro, S. G. M. & E. Olafsson, 1999. Soft-bottom fauna with emphasis on nematode assemblage structure in a tropical intertidal lagoon in Zanzibar, eastern Africa: I. Spatial variability. Hydrobiologia 405: 133-148.

    Google Scholar 

  • Odum, W. E., 1988. Comparative ecology of tidal freshwater and salt marshes. Annual Revue of Ecology and Systematics 19: 147-176.

    Google Scholar 

  • Remane, A. 1958. Ökologie des Brackwassers. In Die Biologie des Brackwassers. Schweizerbartsche Verlag, Stuttgart: 1-213.

  • Rundle, S. D., M. J. Attrill & A. Arshad, 1998. Seasonality in macroinvertebrate community composition across a neglected ecological boundary, the freshwater-estuarine transition zone. Aquatic Ecology 32: 211-216.

    Google Scholar 

  • Seys, J., M. Vincx & P. Meire, 1999. Spatial distribution of oligochaetes (Clitellata) in the tidal freshwater and brackish parts of the Schelde Estuary (Belgium). Hydrobiologia 406: 119-132.

    Google Scholar 

  • Smith, I. M. & D. R. Cook, D. R., 1991. Water mites. In Thorpe, J. H. & A. P. Covich (eds), Ecology and Classification of North American Freshwater Invertebrates. Academic Press, New York: 523-592.

    Google Scholar 

  • Smith, I. M., E. E. Lindquist & V. Behan-Pelletier, 1998. Mites (Acari). In Scudder, G. G. E. & I. M. Smith (eds), Assessment of Species Diversity in the Montane Cordillera Ecozone. Ecological Monitoring and Assessment Network, Burlington, Ontario, Canada: http://www.eman-rese.ca/eman/reports/publications/99_montane/intro.html

  • Stanley, E. H. & J. B. Jones, 2000. Surface-subsurface interactions: past, present, future. In Jones, J. B. & P. J. Mulholland (eds), Streams and Ground Waters. Academic Press, Boston: 405-417.

  • Stoch, F. & P. Pospisil, 2000. Redescription of Diacyclops disjunctus (Thallwitz, 1927) from Austria, with remarks on the Diacyclops languidus-group in Europe (Copepoda, Cyclopoida, Cyclopidae). Crustaceana 73: 469-478.

    Google Scholar 

  • Storey, R. G., K.W. F. Howard & D. D. Williams, 2003. Factors controlling riffle-scale hyporheic exchange flows and their seasonal changes in a gaining stream: a three-dimensional groundwater flow model. Water Resources Research 39: 1-17.

    Google Scholar 

  • ter Braak, C. J. F., 1987-1991. CANOCO: A Fortran programme for canonical community ordination by partial detrended canonical correspondence analysis, principal components analysis and redundancy analysis. Technical Report LWA-88-02, Agricultural & Mathematical Group, Wageningen, The Netherlands, 233 pp.

    Google Scholar 

  • Traunspurger, W, 2002. Nematoda. In Rundle, S. D., A. L. Robertson & J. M. Schmid-Araya (eds), Freshwater Meiofauna: Biology and Ecology. Backhuys Publishers, Leiden: 63-104.

    Google Scholar 

  • Vopel, K., J. Dehmlow & G. Arlt, 1996. Vertical distribution of Cletocamptus confluens (Copepoda, Harpacticoida) in relation to oxygen and sulphide microprofiles of a brackishwater sulphuretum. Marine Ecology Progressive Series 141: 129-137.

    Google Scholar 

  • Warwick, R. M. & R. Price, 1975. Macrofauna production in an estuarine mud-flat. Journal of the Marine Biological Association of the United Kingdom 55: 1-18.

    Google Scholar 

  • Wharfe, J. R., 1977. The intertidal sediment habitats of the lower Medway Estuary, Kent. Environmental Pollution 13: 79-91.

    Google Scholar 

  • Williams, D. D., 1981. Evaluation of a standpipe corer for sampling aquatic interstitial biotopes. Hydrobiologia 83: 257-260.

    Google Scholar 

  • Williams, D. D., 1993. Nutrient and flow vector dynamics at the hyporheic/ groundwater interface and their effects on the interstitial fauna. Hydrobiologia 251: 185-198.

    Google Scholar 

  • Williams, D. D. & T. Hamm, 2002. Insect community organisation in estuaries: the role of the physical environment. Ecography 25: 372-384.

    Google Scholar 

  • Williams, D. D. & H. B. N. Hynes, 1974. The occurrence of benthos deep in the substratum of a stream. Freshwater Biology 4: 233- 256.

    Google Scholar 

  • Williams, D. D. & N. E. Williams, 1998a. Seasonal variation, export dynamics and consumption of freshwater invertebrates in an estuarine environment. Estuarine, Coastal and Shelf Science 46: 393-410.

    Google Scholar 

  • Williams, D. D. & N. E. Williams, 1998b. Aquatic insects in an estuarine environment: densities, distribution and salinity tolerance. Freshwater Biology 39: 411-421.

    Google Scholar 

  • Yozzo, D. J. & R. J. Diaz, 1999. Tidal freshwater wetlands: invertebrate diversity, ecology, and functional significance. In Batzer, D. P., R. B. Rader, & S. A. Wissinger (eds), Invertebrates in Freshwater Wetlands of North America: Ecology and Management. John Wiley & Sons, Inc., New York: 889-918.

    Google Scholar 

  • Ysebaert, T., P. Meire, D. Maes & J. Buijs, 1993. The benthic macrofauna along the estuarine gradient of the Schelde Estuary. Netherlands Journal of Aquatic Ecology 27: 327-341.

    Google Scholar 

  • Ysebaert, T., D. Meire, J. Coosen & K. Essink, 1998. Zonation of intertidal macrobenthos in the estuaries of Schelde and Ems. Aquatic Ecology 32: 53-71.

    Google Scholar 

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Williams, D.D. The brackishwater hyporheic zone: invertebrate community structure across a novel ecotone. Hydrobiologia 510, 153–173 (2003). https://doi.org/10.1023/B:HYDR.0000008642.64116.8f

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