Skip to main content

Advertisement

Log in

Analysis of fatty acid composition of sea cucumber Apostichopus japonicus using multivariate statistics

  • Biology
  • Published:
Chinese Journal of Oceanology and Limnology Aims and scope Submit manuscript

Abstract

Fatty acids (FAs) provide energy and also can be used to trace trophic relationships among organisms. Sea cucumber Apostichopus japonicus goes into a state of aestivation during warm summer months. We examined fatty acid profiles in aestivated and non-aestivated A. japonicus using multivariate analyses (PERMANOVA, MDS, ANOSIM, and SIMPER). The results indicate that the fatty acid profiles of aestivated and non-aestivated sea cucumbers differed significantly. The FAs that were produced by bacteria and brown kelp contributed the most to the differences in the fatty acid composition of aestivated and nonaestivated sea cucumbers. Aestivated sea cucumbers may synthesize FAs from heterotrophic bacteria during early aestivation, and long chain FAs such as eicosapentaenoic (EPA) and docosahexaenoic acid (DHA) that produced from intestinal degradation, are digested during deep aestivation. Specific changes in the fatty acid composition of A. japonicus during aestivation needs more detailed study in the future.

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

  • Alfaro A C, Thomas F, Sergent L, Duxbury M. 2006. Identification of trophic interactions within an estuarine food web (northern New Zealand) using fatty acid biomarkers and stable isotopes. Estuarine, Coastal and Shelf Science, 70(1): 271–286.

    Article  Google Scholar 

  • Anderson M, Gorley R, Clarke K. 2008. PERMANOVA+ for PRIMER: Guide to Software and Statistical Methods. p.1–214.

    Google Scholar 

  • Bachok Z, Mfilinge P L, Tsuchiya M. 2003. The diet of the mud clam Geloina coaxans (Mollusca, Bivalvia) as indicated by fatty acid markers in a subtropical mangrove forest of Okinawa, Japan. Journal of Experimental Marine Biology and Ecology, 292(2): 187–197.

    Article  Google Scholar 

  • Braeckman U, Provoost P, Sabbe K, Soetaert K, Middelburg J, Vincx M, Vanaverbeke J. 2012. Temporal dynamics in macrobenthic diet as inferred from fatty acid biomarkers. Journal of Sea Research, 68(2012): 6–19.

    Article  Google Scholar 

  • Budge S, Parrish C, McKenzie C. 2001. Fatty acid composition of phytoplankton, settling particulate matter and sediments at a sheltered bivalve aquaculture site. Marine Chemistry, 76(4): 285–303.

    Article  Google Scholar 

  • Clarke K R, Gorley R N. 2006. RIMER v6: User Manual Tutorial. Plymouth, UK, PRIMER-E Ltd. p.1–190.

    Google Scholar 

  • Clarke K R, Warwick R M. 2001. Changes in Marine Communities: An Approach to Statistical Analysis and Interpretation, 2nd edn.

    Google Scholar 

  • Colaço A, Desbruyeres D, Guezennec J. 2007. Polar lipid fatty acids as indicators of trophic associations in a deep-sea vent system community. Marine Ecology, 28(1): 15–24.

    Article  Google Scholar 

  • Dalsgaard J, St John M, Kattner G, Müller-Navarra D, Hagen W. 2003. Fatty acid trophic markers in the pelagic marine environment. Advances in Marine Biology, 46: 225–340.

    Article  Google Scholar 

  • Drazen J C, Phleger C F, Guest M A, Nichols P D. 2008. Lipid, sterols and fatty acid composition of abyssal holothurians and ophiuroids from the North-East Pacific Ocean: Food web implications. Comparative Biochemistry and Physiology Part B: Biochemistry and Molecular Biology, 151(1): 79–87.

    Article  Google Scholar 

  • Drazen J C, Phleger C F, Guest M A, Nichols P D. 2009. Lipid composition and diet inferences in abyssal macrourids of the eastern North Pacific. Marine Ecology Progress Series, 387: 1–14.

    Article  Google Scholar 

  • Fernandez-Jover D, Jimenez J A L, Sanchez-Jerez P, Bayle-Sempere J, Casalduero F G, Lopez F J M, Dempster T. 2007. Changes in body condition and fatty acid composition of wild Mediterranean horse mackerel (Trachurus mediterraneus, Steindachner, 1868) associated to sea cage fish farms. Marine Environmental Research, 63(1): 1–18.

    Article  Google Scholar 

  • Gao F, Xu Q, Yang H. 2010. Seasonal variations of food sources in Apostichopus japonicus indicated by fatty acid biomarkers analysis. Journal of Fisheries of China, 34(5): 760–770. (in Chinese with English abstract)

    Article  Google Scholar 

  • Gao F, Xu Q, Yang H. 2011. Seasonal biochemical changes in composition of body wall tissues of sea cucumber Apostichopus japonicus. Chinese Journal of Oceanology and Limnology, 29(2): 252–260.

    Article  Google Scholar 

  • Guest M, Nichols P, Frusher S, Hirst A. 2008. Evidence of abalone (Haliotis rubra) diet from combined fatty acid and stable isotope analyses. Marine Biology, 153(4): 579–588.

    Article  Google Scholar 

  • Hall D, Lee S Y, Meziane T. 2006. Fatty acids as trophic tracers in an experimental estuarine food chain: Tracer transfer. Journal of Experimental Marine Biology and Ecology, 336(1): 42–53.

    Article  Google Scholar 

  • Howell K L, Pond D W, Billett D S M, Tyler P A. 2003. Feeding ecology of deep-sea seastars (Echinodermata: Asteroidea): a fatty-acid biomarker approach. Marine Ecology Progress Series, 255: 193–206.

    Article  Google Scholar 

  • Hughes A D, Catarino A I, Kelly M S, Barnes D K A, Black K D. 2005. Gonad fatty acids and trophic interactions of the echinoid Psammechinus miliaris. Marine Ecology Progress Series, 305: 101–111.

    Article  Google Scholar 

  • Iverson S J. 2009. Tracing aquatic food webs using fatty acids: from qualitative indicators to quantitative determination. In: Lipids in Aquatic Ecosystems. M. T. Arts. Berlin, Heidelberg, Springer. p.281–308.

    Chapter  Google Scholar 

  • Jaschinski S, Brepohl D C, Sommer U. 2011. Seasonal variation in carbon sources of mesograzers and small predators in an eelgrass community: stable isotope and fatty acid analyses. Marine Ecology Progress Series, 431: 69–82.

    Article  Google Scholar 

  • Kelly J R, Scheibling R E. 2012. Fatty acids as dietary tracers in benthic food webs. Marine Ecology Progress Series, 446: 1–22.

    Article  Google Scholar 

  • Mengtan L, Chaolun L, Song S. 2011. Identification of trophic relationships between marine algae and the copepod Calanus sinicus in a fatty acid approach. Acta Ecologica Sinica, 31(4): 933–942. (in Chinese with English abstract)

    Google Scholar 

  • Meziane T, Bodineau L, Retiere C, Thoumelin G. 1997. The use of lipid markers to define sources of organic matter in sediment and food web of the intertidal salt-marsh-flat ecosystem of Mont-Saint-Michel Bay, France. Journal of Sea Research, 38(1–2): 47–58.

    Article  Google Scholar 

  • Parrish C, Abrajano T, Budge S, Helleur R, Hudson E, Pulchan K, Ramos C. 2000. Lipid and Phenolic Biomarkers in Marine Ecosystems: Analysis and Applications. In: Wangersky P ed. The Handbook of Environmental Chemistry. Berlin, Heidelberg, Springer. 5: 193–233.

    Google Scholar 

  • Richoux N B, Froneman P W. 2008. Trophic ecology of dominant zooplankton and macrofauna in a temperate, oligotrophic South African estuary: a fatty acid approach. Marine Ecology Progress Series, 357: 121–137.

    Article  Google Scholar 

  • Soler-Membrives A, Rossi S, Munilla T. 2011. Feeding ecology of Ammothella longipes (Arthropoda: Pycnogonida) in the Mediterranean Sea: a fatty acid biomarker approach. Estuarine Coastal and Shelf Science, 92(4): 588–597.

    Article  Google Scholar 

  • Spector A A. 1999. Essentiality of fatty acids. Lipids, 34: 1–3.

    Article  Google Scholar 

  • Wai T C, Ng J S S, Leung K M Y, Dudgeon D, Williams G A. 2008. The source and fate of organic matter and the significance of detrital pathways in a tropical coastal ecosystem. Limnology and Oceanography, 53(4): 1 479–1 492.

    Article  Google Scholar 

  • Wen X, Ku Y, Zhou K. 2007. Starvation on changes in growth and fatty acid composition of juvenile red swamp crawfish, Procambarus clarkii. Chinese Journal of Oceanology and Limnology, 25(1): 97–105.

    Article  Google Scholar 

  • Yang H, Yuan X, Zhou Y, Mao Y, Zhang T, Liu Y. 2005. Effects of body size and water temperature on food consumption and growth in the sea cucumber Apostichopus japonicus (Selenka) with special reference to aestivation. Aquaculture Research, 36(11): 1 085–1 092.

    Article  Google Scholar 

  • Yang H, Zhou Y, Zhang T, Yuan X, Li X, Liu Y, Zhang F. 2006. Metabolic characteristics of sea cucumber Apostichopus japonicus (Selenka) during aestivation. Journal of Experimental Marine Biology and Ecology, 330(2): 505–510.

    Article  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Hongsheng Yang  (杨红生).

Additional information

Supported by the National Marine Public Welfare Research Project (No. 201305043), the National Natural Science Foundation of China (No. 41106134), and the National Key Technology R&D Program of China (Nos. 2011BAD13B02, 2010BAC68B01)

XU Qinzeng and GAO Fei contributed equally to this work.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Xu, Q., Gao, F., Xu, Q. et al. Analysis of fatty acid composition of sea cucumber Apostichopus japonicus using multivariate statistics. Chin. J. Ocean. Limnol. 32, 1314–1319 (2014). https://doi.org/10.1007/s00343-015-3328-2

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00343-015-3328-2

Keyword

Navigation