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Responses of corophium volutator to sediment sulphide

Published online by Cambridge University Press:  11 May 2009

P. S. Meadows
Affiliation:
Department of Zoology, University of Glasgow, and Department of Applied Microbiology, University of Strathclyde, Glasgow
E. A. Deans
Affiliation:
Department of Zoology, University of Glasgow, and Department of Applied Microbiology, University of Strathclyde, Glasgow
J. G. Anderson
Affiliation:
Department of Zoology, University of Glasgow, and Department of Applied Microbiology, University of Strathclyde, Glasgow

Extract

An apparatus has been developed which allows the complete replacement of interstitial water in sediments without disturbance. In principle, it can be adapted to handle sand or mud, different solutions, and different volumes of sediment. The apparatus was tested with 0·05% (wt/vol.) eosin in sea water. After replacement of the interstitial water, the eosin was evenly distributed throughout the sediment. Interstitial water in samples of sediment was replaced by sulphide solutions in sea water, at a range of concentrations. The responses of Corophium volutator to these sediments was tested in choice and non-choice experiments. In the choice experiments, animals avoided burrowing in sediments containing sulphide at concentrations greater than about 5·8 × 10−5M. In the non-choice experiments, animals were progressively inhibited from burrowing when the sediment sulphide concentration was greater than about 5·8 × 10−4M. No mortality occurred during the experiments.

Type
Research Article
Copyright
Copyright © Marine Biological Association of the United Kingdom 1981

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References

Almgren, T. & Hagstrom, I., 1974. The oxidation rate of sulphide in sea water. Water Research, 8, 395400.CrossRefGoogle Scholar
American Public Health Association, 1971. Standard Methods for the Examination of Water and Waste Water, 13th ed.New York.Google Scholar
Baas, Becking L. G. M., Kaplan, I. R. & Moore, D., 1960. Limits of the natural environment in terms of pH and oxidation-reduction potentials. Journal of Geology, 68, 243284.Google Scholar
Blackburn, T. H., Kleiber, P. & Fenchel, T., 1975. Photosynthetic sulfide oxidation in marine sediments. Oikos, 26, 103108.CrossRefGoogle Scholar
Boaden, P. J. S., 1968. Water movement - a dominant factor in interstitial ecology. Sarsia, 34, 125136.Google Scholar
Fenchel, T., Kofoed, L. H. & Lappalainen, A., 1975. Particle size-selection of two deposit feeders: the amphipod Corophium volutator and the prosobranch Hydrobia ulvae. Marine Biology, 30, 119128.CrossRefGoogle Scholar
Fenchel, T. M. & Riedl, R. J., 1970. The sulfide system: a new biotic community underneath the oxidised layer of marine sand bottoms. Marine Biology, 7, 255268.CrossRefGoogle Scholar
Hallberg, R. O., 1973. The microbiological C-N-S cycles in sediments and their effect on the ecology of the sediment-water interface. Oikos, 15, 5162.Google Scholar
Hecht, F., 1932. Der chemische Einfluss organischer Zersetzungsstoffe auf das Benthos, dargelegt an Untersuchungen mit marinen Polychaeten, insbesondere Arenicola marina L. Senckenbergiana, 14, 199220.Google Scholar
Jacubowa, L. & Malm, E., 1931. Die Beziehungen einiger Benthos-formen des Schwarzen meeres zum Medium. Biologisches Zentralblatt, 51, 105116.Google Scholar
Jorgensen, B. B., 1977. The sulfur cycle of a coastal marine sediment (Limf jorden, Denmark). Limnology and Oceanography, 22, 814832.CrossRefGoogle Scholar
Meadows, P. S., 1964. Substrate selection by Corophium species: the particle size of substrates. Journal of Animal Ecology, 33, 387394.CrossRefGoogle Scholar
Meadows, P. S. & Cambpell, J. I., 1972. Habitat selection and animal distribution in the sea: the evolution of a concept. Proceedings of the Royal Society of Edinburgh (B), 73, 145157.Google Scholar
Nedwell, D. B. & Floodgate, G. D., 1972. The effects of microbial activity upon the sedimentary sulphur cycle. Marine Biology, 16, 192200.CrossRefGoogle Scholar
Ostlund, H. G. & Alexander, J. 1963. Oxidation rate of sulfide in sea water, a preliminary study. Journal of Geophysical Research, 68, 39953997.Google Scholar
Ramm, A. E. & Bella, D. A., 1974. Sulfide production in anaerobic microcosms. Limnology and Oceanography, 19, 110118.CrossRefGoogle Scholar
Shick, J. M., 1976. Physiological and behavioural responses to hypoxia and hydrogen sulfide in the infaunal asteroid Ctenodiscus crispatus. Marine Biology, 37, 279289.Google Scholar
Sokal, R. R. & Rohlf, F. J., 1969. Biometry. 776 pp. San Francisco: Freeman.Google Scholar
Theede, H., 1973. Comparative studies on the influence of oxygen deficiency and hydrogen sulphide on marine bottom invertebrates. Netherlands Journal of Sea Research, 7, 244252.Google Scholar
Theede, H., Ponat, A., Hiroki, K. & Schlieper, C, 1969. Studies on the resistance of marine bottom invertebrates to oxygen-deficiency and hydrogen sulphide. Marine Biology, 2, 325337.CrossRefGoogle Scholar
Wheatland, A. B., 1954. Factors affecting the formation and oxidation of sulphides in a polluted estuary. Journal of Hygiene, Cambridge, 52, 194210.CrossRefGoogle Scholar