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Latitudinal Variation of Nutritional Condition and Diet for Copepod Species, Euchaeta sp. and Pleuromamma spp., from the Northwest Pacific Ocean Using Lipid Biomarkers

지방 바이오마커를 활용한 북서태평양에서 요각류(Euchaeta sp. and Pleuromamma spp.)의 서식 위도별 영양상태 및 먹이원 연구

  • Ju, Se-Jong (Deep-sea and Marine Georesources Research Department, KORDI) ;
  • Ko, Ah-Ra (Deep-sea and Marine Georesources Research Department, KORDI) ;
  • Lee, Chang-Rae (National Park Research Institute, Korea National Park Service)
  • 주세종 (한국해양연구원 심해해저자원연구부) ;
  • 고아라 (한국해양연구원 심해해저자원연구부) ;
  • 이창래 (국립공원관리공단 국립공원연구원)
  • Received : 2011.07.13
  • Accepted : 2011.09.01
  • Published : 2011.09.30

Abstract

In order to ascertain latitudinal variation of lipid contents and compositions in copepods, we collected warm water copepod species (Euchaeta sp. and Pleuromamma spp.) from four different regions from low (sub-tropical) to mid (temperate) latitudes in the Northwest Pacific Ocean. Total lipid contents of Pleuromamma spp. were about 11 $ug{\cdot}ind^{-1}$ with little latitudinal variation, whereas Euchaeta sp. showed slightly higher lipid content (20 $ug{\cdot}ind^{-1}$) than Pleuromamma spp. with latitudinal gradient (low at subtropic and high at temperate). Wax esters, known as the major storage lipid classes, were found to be the dominant lipid classes (accounting for more than 35% of total lipids) in Euchaeta sp., whereas in Pleuromamma spp., phospholipids, known as cellular membrane components, were the dominant lipid classes. However, the exception was specimens from warm pool region exhibiting dominance in storage of lipids as a form of triacylglycerols. Among fatty acids, polyunsaturated fatty acids (PUFA), especially docosahexaenoic acid (DHA : 22:6(n-3)) (about 35% of total fatty acids), were most abundant in Euchaeta sp., while saturated fatty acids (SAFA), specially hexadecanoic acid (16:0) (about 30% of total fatty acids), were most abundant in Pleuromamma spp.. Among the neutral fraction of lipids, phytol, originated from the side chain of chlorophyll, was found in all samples which generally indicate active copepods feeding on algae. While only trace amounts of short-chain fatty alcohols were found in Pleuromamma spp., significant amounts of fatty alcohols were found in Euchaeta sp.. Particularly, significant amounts of long chain monounsaturated fatty alcohols (20:1 and 22:1), generally found in cold water species, were found in Euchaeta sp. from low latitudes. The latitudinal variation of trophic lipid markers in these copepods could be significantly related with in-situ food availability and species-specific diet preference. The result of this study suggests that the lipid contents and compositions in copepods may not only indicate their nutritional condition and feeding ecology but also provide insight into species-specific living strategies under different environmental conditions (i.e. water temperature, food availability).

Keywords

References

  1. 최동림, 노재훈, 유주형, 이재학, 장풍국, 이태희, 최동한 (2010) 2008년 여름철 북부 동중국해에서 대규모 녹조(가시파래) 출현. Ocean and Polar Res 32(4):351-359 https://doi.org/10.4217/OPR.2010.32.4.351
  2. 한국해양연구원 (2008) 북서 태평양이 한반도 주변해(대한해협)에 미치는 영향 연구. 한국해양연구원, BSPP07401-1917-1, 783 p
  3. Albers CS, Kattner G, Hagen W (1996) The composition of wax esters, triacylglycerols and phospholipids in Arctic and Antarctic copepods: evidence of energetic adaptations. Mar Chem 55:347-358 https://doi.org/10.1016/S0304-4203(96)00059-X
  4. Ambler JW, Miller CB (1987) Vertical habotat-partitioning by copepodites and adults of subtropical oceanic copepods. Mar Biol 94:561-577 https://doi.org/10.1007/BF00431403
  5. Auel H, Harjes M, da Rocha R, Stubing D, Hagen W (2002) Lipid biomarkers indicate different ecological niches and trophic relationships of the Arctic hyperiid amphipods Themisto abyssorum and T. libellula. Polar Biol 25:374-383
  6. Benson AA, Lee RF (1975) The role of wax in oceanic food chains. Sci Am 232:77-83
  7. Bligh EG, Dyer WJ (1959) A rapid method of total lipid extraction and purification. Can J Biochem Physiol 37:911-917 https://doi.org/10.1139/o59-099
  8. Bougis P (1976) Marine Plankton Ecology. Elsevier, New York, 169 p
  9. Cripps GC, Atkinson A (2000) Fatty acid composition as an indicator of carnivory in Antarctic krill, Euphausia superba. Can J Fish Aquat Sci 57:31-37
  10. Dalsgaard J, St. John M, Kattner G, Muller-Navarra D, Hagen W (2003) Fatty acid trophic markers in the pelagic marine environment. Adv Mar Biol 46:225-340 https://doi.org/10.1016/S0065-2881(03)46005-7
  11. Destaillats F, Angers P (2002) Base-catalyzed derivatization methodology for FA analysis. application to milk fat and celery seed lipid TAG. Lipids 37(5):527-532 https://doi.org/10.1007/s11745-002-0928-9
  12. Ederington MC, McManus GB, Harvey HR (1995) Trophic transfer of fatty acids, sterols, and a triterpenoid alcohol between bacteria, a ciliate, and the copepod Acartia tonsa. Limnol Oceanogr 40:860-867 https://doi.org/10.4319/lo.1995.40.5.0860
  13. El-Sabaawi R, Dower JF, Kainz M, Mazumder A (2009) Characterizing dietary variability and trophic positions of coastal calanoid copepods: insight from stable isotopes and fatty acids. Mar Ecol Prog Ser 156:225-237
  14. Falk-Petersen S, Hagen W, Kattner G, Clarke A, Sargent JR (2000) Lipids, trophic relationships, and biodiversity in Arctic and Antarctic krill. Can J Fish Aquat Sci 57:178-191 https://doi.org/10.1139/f00-194
  15. Barnes M, Gibson RN (1990) Trophic relationships in marine environments: proceedings of the 24th European Marine Biology Symposium. Aberdeen University Press, Aberdeen, 642 p
  16. Fowler SW, Knauer GA (1986) Role of large particles in the transport of elements and organic compounds through the oceanic water column. Prog Oceanogr 16:147-194 https://doi.org/10.1016/0079-6611(86)90032-7
  17. Frost BW, Landary MR, Hassett RP (1983) Feeding behavior of large calanoid copepods Neocalanus cristantus and N. plumchrus from the subarctic Pacific Ocean. Deep-Sea Res I 30:1-13
  18. Goad LJ (1978) The sterols of marine invertebrates: composition, biosynthesis and metabolites. In: Scheure PJ (ed) Marine natural products, Academic Press, New York, pp 74-172
  19. Graeve M, Kattner G, Hagen W (1994) Diet-induced changes in the fatty acid composition of Arctic herbivorous copepods: experimental evidence of trophic markers. J Exp Mar Biol Ecol 182:97-110 https://doi.org/10.1016/0022-0981(94)90213-5
  20. Hagen W, Van Vleet ES, Kattner G (1996) Seasonal lipid storage as overwintering strategy of Antarctic krill. Mar Ecol Prog Ser 134:85-89 https://doi.org/10.3354/meps134085
  21. Hayward TL (1980) Spatial and temporal feedong patterns of copepods from the North Pacific Central Gyre. Mar Biol 56:295-309 https://doi.org/10.1007/BF00386867
  22. Ju S-J, Harvey HR (2004) Lipids as markers of nutritional condition and diet in the Antarctic krill Euphausia superba and E. crystallorophias during austral winter. Deep-Sea Res II 51:2199-2214 https://doi.org/10.1016/j.dsr2.2004.08.004
  23. Ju S-J, Kang H-K, Kim WS, Harvey HR (2009) Comparative lipid dynamics of euphausiids from Antarctic and Northeast Pacific Oceans. Mar Biol 156:1459-1473 https://doi.org/10.1007/s00227-009-1186-1
  24. Ju S-J, Kucklick JR, Kozlova T, Harvey HR (1997) Lipid accumulation and fatty acid composition during maturation of three pelagic fish species in Lake Baikal. J Great Lakes Res 23(3):241-253 https://doi.org/10.1016/S0380-1330(97)70909-2
  25. Kattner G, Hagen W, Graeve M, Albers C (1998) Exceptional lipids and fatty acids in the pteropod Clione limacina (Gastropoda) from both polar oceans. Mar Chem 61:219-228 https://doi.org/10.1016/S0304-4203(98)00013-9
  26. Kattner G, Hagen W (2010) Lipids in marine copepods: latitudinal characteristics and perspective to global warming. In: Arts MT, Brett MT, Kainz MJ (eds) Lipids in Aquatic ecosystem, Springer, London, pp 257-280
  27. Lee RF, Nevenzel JC, Paffenhfer GA (1970) Wax esters in marine copepods. Science 167:1510-1511 https://doi.org/10.1126/science.167.3924.1510
  28. Lee RF, Hagen W, Kattner G (2006) Lipid storage in marine zooplankton. Mar Ecol Prog Ser 307:273-306 https://doi.org/10.3354/meps307273
  29. Ikeda T (1974) Nutritional ecology of marine zooplankton. Mem Fac Fish Hokkaido Univ 22:1-97
  30. Mackey DJ, Parslow J, Griffiths FB, Higgins HW, Tilbrook B (1997) Phytoplankton productivity and the carbon cycle in the western Equatorial Pacific under El Nino and non-El Nino conditions. Deep-Sea Res II 44:1951-1978 https://doi.org/10.1016/S0967-0645(97)00033-7
  31. Mayzaud P, Boutoute M, Alonzo F (2003) Lipid composition of the Antarctic euphausiids Euphausia vallentini and Thysanoessa macrura during summer in the Indian sector of the Southern ocean. Antarctic Sci 15:463-475 https://doi.org/10.1017/S0954102003001573
  32. Michener RH, Kaufman L (2007) Stable isotope ratios as tracers in marine food webs: an update. In: Michener RH, Lajitha K (eds) Stable isotopes in ecology and environmental science. Blackwell Publishing Ltd., Oxford, pp 238-282
  33. Nichols PD, Guckert JB, White DC (1986) Determination of monosaturated fatty acid double-bond position and geometry for microbial monocultures and complex consortia by capillary GC-MS of their dimethyl disulphide adducts. J Microbiol Meth 5(1):49-55 https://doi.org/10.1016/0167-7012(86)90023-0
  34. Rampen SW, Abbas BA, Schouten S, Damste JSS (2010) A comprehensive study of sterols in marine diatoms (Bacillariophyta): implications for their use as tracers for diatom productivity. Limnol Oceanogr 55(1):91-105 https://doi.org/10.4319/lo.2010.55.1.0091
  35. Sargent JR, Henderson RJ (1986) Lipids. In: Corner EDS and O'Hara SCM (eds) The biological chemistry of marine copepods, Clarendon Press, London, pp 59-108
  36. Schnetzer A, Steinberg DK (2002) Natural diets of vertical migrating zooplankton in the Sargasso Sea. Mar Biol 141:89-99 https://doi.org/10.1007/s00227-002-0815-8
  37. Swalethorp R, Kjellerup S, Dunweber M, Nielsen TG, Moller EF, Rysgaard S, Hansen BW (2011) Grazing, egg production, and biochemical evidence of differences in the life strategies of Calanus finmarchicus, C. glacialis and C. hyperboreus in Disko Bay, western Greenland. Mar Ecol Prog Ser 429:125-144 https://doi.org/10.3354/meps09065
  38. Volkman JK, Barrett SM, Blackburn SI, Mansour MP, Sikes EL, Gelin F (1998) Microalgal biomarkers: a review of recent research developments. Org Geochem 29(5-7): 1163-1179 https://doi.org/10.1016/S0146-6380(98)00062-X
  39. Wada E, Hattori A (1991) Nitrogen in the sea: forms, abundances, and rate processes. CRC press, Boston, 208 p
  40. Yen J (1988) Directionality and swimming speeds in predator-prey and male-female interactions of Euchaeta rimana, a subtropical marine copepod. Bull Mar Sci 43(3):395-403

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