Skip to main content
Log in

Differences in microhabitat, abundance, biomass and body size between oxybiotic and thiobiotic free-living marine nematodes

  • Original Papers
  • Published:
Oecologia Aims and scope Submit manuscript

Summary

Analysis of samples from a 15 m deep sandy bottom in the northern part of Øresund, Denmark shows that the nematode fauna comprises 2.9 million individuals per m2 down to 20 cm depth which averages of 0.40 g organic carbon. Highest densities are found in the uppermost cm. Biomass attains its highest value at 1–2 cm depth. Three results are discussed: 1) nematodes in the uppermost cm are, on average, three times smaller than those between 1–8 cm depth (60 ng org. C vs. 200 ng org. C ind. weight); 2) a distinct abundance trough is found at 8 cm depth, which correlates with the physical space occupied by the gallery of the lugworm Arenicola marina as well as with its possibly unselective feeding on the interstitial meiofauna at that depth; 3) the thiobiotic (deeper-living) species are significantly more slender than the oxybiotic (surface-dwelling) species, suggesting surface-dependent adaptations to life in oxygen poor and sulphide rich sediments where large amounts of dissolved organic matter occur. This is in contrast to previous assumptions that the body length or body shape reflects adaptations to the physical constraints of interstitial space.

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.

Similar content being viewed by others

References

  • Andrassy I (1956) Die Rauminhalts-und Gewichtsbestimmung der Fadenwürmer (Nematoden). Acta zool Hung 11:1–5

    Google Scholar 

  • Arlt G (1973) Vertical and horizontal microdistribution of the meiofauna in the Greifswalder Bodden. Oikos suppl 15:105–111

    Google Scholar 

  • Boaden PJS, Platt HM (1971) Daily migration patterns in an intertidal meiobenthic community. Thalassia jugosl 7:1–12

    Google Scholar 

  • Fenchel T, Riedl RJ (1970) The sulfide system: a new biotic community underneath the oxidized layer of marine sand bottoms. Mar Biol 7:255–268

    Google Scholar 

  • Gerlach SA (1958) Die Nematodenfauna der sublitoralen Region in der Kieler Bucht. Kieler Meeresforsch 14:64–90

    Google Scholar 

  • Gerlach SA, Hahn AE, Schrage M (1985) Size spectra of benthic biomass and metabolism. Mar Ecol Prog Ser 26:161–173

    Google Scholar 

  • Heip C, Vincx M, Vranken G (1985) The ecology of marine nematodes. Oceanogr Mar Biol Ann Rev 23:399–489

    Google Scholar 

  • Hylleberg J (1975) Selective feeding by Abarenicola pacifica with notes on Abarenicola vagabunda and a concept of gardening in lugworms. Ophelia 14:113–137

    Google Scholar 

  • Jensen P (1980) Description of the marine free-living nematode Chromadora lorenzeni n. sp., with notes on its microhabitats. Zool Anz 205:213–218

    Google Scholar 

  • Jensen P (1982) A new meiofauna sample splitter. Ann zool Fenn 19:233–236

    Google Scholar 

  • Jensen P (1984) Measuring carbon content in nematodes. Helgoländer Meeresunters 38:83–86

    Google Scholar 

  • Jensen P (1986) Nematode fauna in the sulphide-rich brine seep and adjacent bottoms of the East Flower Garden, NW Gulf of Mexico. IV. Ecological aspects. Mar Biol 92:489–503

    Google Scholar 

  • Joint IR, Gee JM, Warwick RM (1982) Determinations of finescale vertical distribution of microbes and meiofauna in an intertidal sediment. Mar Biol 72:157–164

    Google Scholar 

  • Jørgensen BB (1977) Bacterial sulfate reduction within reduced microniches of oxidized marine sediments. Mar Biol 41:7–17

    Google Scholar 

  • Powell EN, Bright TJ, Woods A, Gittins S (1983) Meiofauna and the thiobios in the East Flower Garden brine seep. Mar Biol 73:269–283

    Google Scholar 

  • Reise K, Ax P (1979) A meiofauna “thiobios” limited to the anaerobic sulfide system of marine sand does not exist. Mar Biol 54:225–237

    Google Scholar 

  • Reise K, Ax P (1980) Statement on the thiobios-hypothesis. Mar Biol 58:31–32

    Google Scholar 

  • Remane A (1933) Verteilung und Organisation der benthonischen Mikrofauna der Kieler Bucht. Wiss Meeresunters Kiel NF 21:161–221

    Google Scholar 

  • Remane A (1942) Die Bedeutung der Lebensformtypen für die Ökologie. Biol gener 17:164–182

    Google Scholar 

  • Revsbech NP, Jørgensen BB, Blachburn TH, Cohen Y (1983) Microelectrode studies of the photosynthesis and O2, H2S and pH profiles of a microbial mat. Limnol Oceanogr 28:1062–1074

    Google Scholar 

  • Warwick RM, Gee JM (1984) Community structure of estuarine meiobenthos. Mar Ecol Prog Ser 18:97–111

    Google Scholar 

  • Wieser W (1975) The meiofauna as a tool in the study of habitat heterogeneity: ecophysiological aspects. A review. Cah Biol Mar 16:647–670

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Jensen, P. Differences in microhabitat, abundance, biomass and body size between oxybiotic and thiobiotic free-living marine nematodes. Oecologia 71, 564–567 (1987). https://doi.org/10.1007/BF00379298

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00379298

Key words

Navigation