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A new method to determine the reproductive condition in female tubeworms tested in Seepiophila jonesi (Polychaeta: Siboglinidae: Vestimentifera)

Published online by Cambridge University Press:  24 June 2008

Ana Hilário*
Affiliation:
School of Ocean and Earth Science, University of Southampton, National Oceanography Centre, European Way, SO14 3ZH, Southampton, UK Present address: CESAM, Departamento de Biologia, Campus Universitário de Santiago, 3810-193 Aveiro, Portugal
Paul A. Tyler
Affiliation:
School of Ocean and Earth Science, University of Southampton, National Oceanography Centre, European Way, SO14 3ZH, Southampton, UK
David W. Pond
Affiliation:
Biological Sciences Division, British Antarctic Survey, High Cross, Madingley Road, CB3 0ET, Cambridge, UK
*
Correspondence should be addressed to: Ana HilárioCESAM, Departamento de Biologia Universidade de AveiroCampus Universitário de Santiago 3810-193 Aveiro, Portugal email: [email protected]

Abstract

Vestimentiferan tubeworms are significant members of deep-sea chemosynthetically-driven communities, including hydrothermal vents and cold seeps. The reproductive condition in this taxon is rarely studied because of sampling constraints inherent to these environments, and the lack of a simple methodology to quantify gonad development in vestimentiferans.

We demonstrate that the amount of gonad found in the first 10 mm of trunk can be used as representative of the reproductive condition of the individual, and we establish a linear relationship between the amount of gonad and the proportion of wax ester in the trunk of female vestimentiferans. This relationship represents a new method for the determination of the reproductive condition in this group.

Type
Research Article
Copyright
Copyright © Marine Biological Association of the United Kingdom 2008

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References

REFERENCES

Allen, C.E. (1998) Lipid profiles of deep-sea organisms. PhD thesis, School of Ocean and Earth Science, University of Southampton.Google Scholar
Copley, J.T.P. and Young, C.M. (2006) Seasonality and zonation in the reproductive biology and population structure of the shrimp Alvinocaris stactophila (Caridea: Alvinocarididae) at a Louisiana Slope cold seep. Marine Ecology Progress Series 315, 199209.CrossRefGoogle Scholar
Copley, J.T.P., Tyler, P.A., Van Dover, C.L. and Philp, S. (2003) Spatial variation in the reproductive biology of Paralvinella palmiformis (Polychaeta: Alvinellidae) from a vent field on Juan de Fuca Ridge. Marine Ecology Progress Series 255, 171181.CrossRefGoogle Scholar
Folch, J., Lees, M. and Sloane-Stanley, G.H. (1957) A simple method for the isolation and purification of total lipids from animal tissues. Journal of Biological Chemistry 226, 497509.CrossRefGoogle ScholarPubMed
Gardiner, S.L., McMullin, E. and Fisher, C.R. (2001) Seepiophila jonesi, a new genus and species of vestimentiferan tubeworm (Annelida: Pogonophora) from hydrocarbon seep communities in the Gulf of Mexico. Proceedings of the Biological Society of Washington 114, 694707.Google Scholar
Hilário, A., Young, C.M. and Tyler, P.A. (2005) Sperm storage, internal fertilization and embryonic dispersal in vent and seep tubeworms (Polychaeta: Siboglinidae: Vestimentifera). Biological Bulletin. Marine Biological Laboratory, Woods Hole 208, 2028.CrossRefGoogle ScholarPubMed
Jeckel, W.H., de Moreno, J.E.A. and Moreno, V.J. (1989) Biochemical composition, lipid classes and fatty acids in the ovary of the shrimp Pleoticus muelleri Bate. Comparative Biochemistry and Physiology B 92, 271276.CrossRefGoogle Scholar
Marsh, A.G., Mullineaux, L.S, Young, C.M. and Manahan, D.T. (2001) Larval dispersal potential of the tubeworm Riftia pachyptila at deep-sea hydrothermal vents. Nature 411, 7780.CrossRefGoogle ScholarPubMed
Olsen, R.E. and Henderson, R.H. (1989) The rapid analysis of neutral and polar marine lipids using double-development HPTLC and scanning densitometry. Journal of Experimental Marine Biology and Ecology 129, 189197.CrossRefGoogle Scholar
Perovich, G.M., Epifanio, C.E., Dittel, A.I. and Tyler, P.A. (2003) Spatial and temporal patterns in development of eggs in the vent crab Bythograea thermydron. Marine Ecology Progress Series 251, 211220.CrossRefGoogle Scholar
Tyler, P.A. and Young, C.M. (1999) Reproduction and dispersal at vents and cold seeps. Journal of the Marine Biological Association of the United Kingdom 79, 193208.CrossRefGoogle Scholar
Young, C.M., Vásquez, E., Metaxas, A. and Tyler, P.A. (1996) Embryology of vestimentiferan tube worms from deep-sea methane/sulfide seeps. Nature 381, 514516.CrossRefGoogle Scholar