Hostname: page-component-586b7cd67f-t7czq Total loading time: 0 Render date: 2024-11-24T22:00:00.304Z Has data issue: false hasContentIssue false
  • English
  • Français

Fine structure of the tubes of Maldanidae (Annelida)

Published online by Cambridge University Press:  10 August 2017

Tatiana D. Shcherbakova ,
Alexander B. Tzetlin ,
Maria V. Mardashova  and
Olga S. Sokolova
Tatiana D. Shcherbakova*
Affiliation:
M.V. Lomonosov Moscow State University, Leninskie Gory, 1–12, Moscow 119991, Russia
Alexander B. Tzetlin
Affiliation:
M.V. Lomonosov Moscow State University, Leninskie Gory, 1–12, Moscow 119991, Russia
Maria V. Mardashova
Affiliation:
M.V. Lomonosov Moscow State University, Leninskie Gory, 1–12, Moscow 119991, Russia
Olga S. Sokolova
Affiliation:
M.V. Lomonosov Moscow State University, Leninskie Gory, 1–12, Moscow 119991, Russia
*
Correspondence should be addressed to: T. D. Shcherbakova, M.V. Lomonosov Moscow State University, Leninskie Gory, 1–12, Moscow 119991, Russia email: [email protected]
Get access Rights & Permissions [Opens in a new window]

Abstract

Many marine annelids are active tube builders. Several polychaete families make agglutinated tubes by fixing sediment particles with specific secretions from their epithelial glands. The fine structure of the tubes of six species of Maldanidae from five genera (Nicomache minor, N. lumbricalis, Maldane sarsi, Praxillella praetermissa, Axiothella catenata, Rhodine gracilior) was examined by scanning electron microscopy. These species exhibit different lifestyles. Nicomache minor and N. lumbricalis inhabit massive hard tubes attached to stones. Other species live in the sediment, Rhodine in rigid organic tubes, Praxillella, Axiothella and Maldane in sand or mud tubes. All the examined maldanid tubes have a similar basic structure. The inner sheath of the tubes is made of a hardened organic lining secreted by the worm. Fibres from the inner sheath fasten sediment particles of the agglutinated layer. In Nicomache the tube surface is covered with a fibrous outer layer. All tube layers contain variously arranged organic fibres, which form a 3D network in the agglutinated layer and fabric-like linings in the inner sheath and outer layer. The tubes of Maldanidae may be important for taxonomy, and useful for identification of fossils.

Keywords

PolychaetaMaldanidaeagglutinated tubestube structureSEM
Type
Research Article
Information
Journal of the Marine Biological Association of the United Kingdom , Volume 97 , Special Issue 5: Proceedings of the 12th International Polychaete Conference Amgueddfa Cymru - National Museum Wales Cardiff, Wales, UK, 1-5 August 2016 , August 2017 , pp. 1177 - 1187
Copyright
Copyright © Marine Biological Association of the United Kingdom 2017 

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

Barnes, R.D. (1965) Tube-building and feeding in chaetopterid polychaetes. The Biological Bulletin 129, 217–233.Google Scholar
Bolam, S.G. and Fernandes, T.F. (2002) Dense aggregations of tube-building polychaetes: response to small-scale disturbances. Journal of Experimental Marine Biology and Ecology 269, 197–222.CrossRefGoogle Scholar
Bonar, D.B. (1972) Feeding and tube construction in Chone mollis Bush (Polychaeta, Sabellidae). Journal of Experimental Marine Biology and Ecology 9, 1–18.Google Scholar
Budaeva, N., Pyataeva, S. and Meißner, K. (2014) Development of the deep-sea viviparous quill worm Leptoecia vivipara (Hyalinoeciinae, Onuphidae, Annelida). Invertebrate Biology 133, 242–260.Google Scholar
Dean, M., Welch, J., Brandt, C. and Tauer, T. (2009) Surface analyses of biocements from Pectinaria gouldii (Polychaeta: Pectinariidae) and Phragmatopoma lapidosa (Polychaeta: Sabellariidae). In Maciolek, N.J. and Blake, J.A. (eds) Proceedings of the 9th International Polychaete Conference, Portland, Maine, USA 2007. Zoosymposia 2, 329–337.Google Scholar
Defretin, R. (1971) The tubes of polychaete annelids. Comprehensive Biochemistry 26, 713–747.Google Scholar
Desroy, N., Olivier, F. and Retière, C. (1997) Effects of individual behaviors, inter-individual interactions with adult Pectinaria koreni and Owenia fusiformis (Annelida, Polychaeta), and hydrodynamism on Pectinaria koreni recruitment. In Reish, D.J. and Qian, P.-Y. (eds) Proceedings of the 5th International Polychaete Conference, Qingdao, China 1995. Bulletin of Marine Science 60, 547–558.Google Scholar
Dudgeon, D. (1994) The functional significance of selection of particles by aquatic animals during building behaviour. In Wotton, R.S. (ed.) The biology of particles in aquatic systems, 2nd edition. Boca Raton, FL: Lewis Publishers, pp. 289–312.Google Scholar
Dufour, S.C., White, C., Desrosiers, G. and Juniper, S.K. (2008) Structure and composition of the consolidated mud tube of Maldane sarsi (Polychaeta: Maldanidae). Estuarine, Coastal and Shelf Science 78, 360–368.Google Scholar
Fager, E.W. (1964) Marine sediments: effects of a tube-building polychaete. Science 143, 356–358.Google Scholar
Fauchald, K. and Jumars, P.A. (1979) The diet of worms: a study of polychaete feeding guilds. Oceanography and Marine Biology. An Annual Review 17, 193–284.Google Scholar
Flammang, P. and Lambert, A. (2008) Cement ultrastructure and adhesive glands morphology in the tube-dwelling polychaete Sabellaria alveolata . Journal of Morphology 269, 1479.Google Scholar
Hughes, T.G. (1979) Mode of life and feeding in maldanid polychaetes from St. Margaret's Bay, Nova Scotia. Journal of the Fisheries Research Board of Canada, 36, 1503–1507.Google Scholar
Jumars, P.A., Dorgan, K.M. and Lindsay, S.M. (2015) Diet of worms emended: an update of polychaete feeding guilds. Annual Review of Marine Science 7, 497–520.Google Scholar
Knox, G.A. (1977) The role of polychaetes in benthic soft-bottom communities. In Reish, D.J. and Fauchald, K. (eds) Essays on polychaetous annelids in memory of Dr. Olga Hartman. Allan Hancock Foundation Special Publication. Los Angeles, CA: University of Southern California Press, pp. 547–604.Google Scholar
Kongsrud, J.A. and Rapp, H.T. (2012) Nicomache (Loxochona) lokii sp. nov. (Annelida: Polychaeta: Maldanidae) from the Loki's Castle vent field: an important structure builder in an Arctic vent system. Polar Biology 35, 161–170.Google Scholar
Kristensen, E., Penha-Lopes, G., Delefosse, M., Valdemarsen, T., Quintana, C. and Banta, G. (2012) What is bioturbation? The need for a precise definition for fauna in aquatic sciences. Marine Ecology Progress Series 446, 285–302.Google Scholar
Kudenov, J.D. (1978) The feeding ecology of Axiothella rubrocincta (Johnson) (Polychaeta: Maldanidae). Journal of Experimental Marine Biology and Ecology 31, 209–221.Google Scholar
Kudenov, J.D. (1982) Rates of seasonal sediment reworking in Axiothella rubrocincta (Polychaeta: Maldanidae). Marine Biology 70, 181–186.Google Scholar
Le Cam, J.B., Fournier, J., Etienne, S. and Couden, J. (2011) The strength of biogenic sand reefs: Visco-elastic behaviour of cement secreted by the tube building polychaete Sabellaria alveolata, Linnaeus, 1767. Estuarine, Coastal and Shelf Science 91, 333–339.Google Scholar
Mangum, C.P. (1964) Studies on speciation in maldanid polychaetes of the North American Atlantic coast. II. Distribution and competitive interaction of five sympatric species. Limnology and Oceanography 9, 12–26.Google Scholar
McIntosh, W.C. (1894) On certain homes or tubes formed by Annelids. The Annals and Magazine of Natural History, Series 6 13, 1–18.Google Scholar
Mermillod-Blondin, F. (2011) The functional significance of bioturbation and biodeposition on biogeochemical processes at the water–sediment interface in freshwater and marine ecosystems. Journal of the North American Benthological Society 30, 770–778.CrossRefGoogle Scholar
Merz, R.A. (2015) Textures and traction: how tube-dwelling polychaetes get a leg up. Invertebrate Biology 134, 61–77.Google Scholar
Noffke, A., Hertweck, G., Kröncke, I. and Wehrmann, A. (2009) Particle size selection and tube structure of the polychaete Owenia fusiformis . Estuarine, Coastal and Shelf Science 81, 160–168.Google Scholar
Rouse, G.W. (1992) Oogenesis and larval development in Micromaldane spp. (Polychaeta: Capitellida: Maldanidae). Invertebrate Reproduction and Development 21, 215–230.Google Scholar
Shcherbakova, T.D. and Tzetlin, A.B. (2016) Fine structure of agglutinated tubes of polychaetes of the family Terebellidae (Annelida). Doklady Biological Sciences 466, 16–20.Google Scholar
Stewart, R.J., Ransom, T.C. and Hlady, V. (2011) Natural underwater adhesives. Journal of Polymer Science Part B: Polymer Physics 49, 757–771.Google Scholar
Tzetlin, A.B. and Markelova, N.P. (1985) Some aspects of the distribution and biology of Nicomache minor (Polychaeta: Maldanidae) in the White Sea. Explorations of the Fauna of the Seas 34, 136–138.Google Scholar
Vinn, O. (2009) The ultrastructure of calcareous cirratulid (Polychaeta, Annelida) tubes. Estonian Journal of Earth Sciences 58, 153–156.Google Scholar
Vinn, O. and Luque, J. (2013) First record of a pectinariid-like (Polychaeta, Annelida) agglutinated worm tube from the Late Cretaceous of Colombia. Cretaceous Research 41, 107–110.Google Scholar
Watson, A.T. (1901) On the structure and habits of the Polychaeta of the family Ammocharidae. Zoological Journal of the Linnean Society 28, 230–260.Google Scholar
Wilson, W.H. Jr. (1983) Life-history evidence for sibling species in Axiothella rubrocincta (Polychaeta: Maldanidae). Marine Biology, Berlin 76, 297–300.Google Scholar
Zhao, H., Sun, C., Stewart, R.J. and Waite, J.H. (2005) Cement proteins of the tube-building polychaete Phragmatopoma californica . Journal of Biological Chemistry 280, 42938–42944.Google Scholar