DOI QR코드

DOI QR Code

The Physiological and Ecological Comparisons between Warm (Pleuromamma sp.) and Cold Water Copepod Species (Neocalanus plumchrus) in the Northwestern Pacific Ocean Using Lipid Contents and Compositions

북서태평양에서 난수성(Pleuromamma sp.)과 냉수성(Neocalanus plumchrus) 요각류의 지방 함량 및 구성 분석을 통한 생리/생태 비교

  • Ko, Ah-Ra (Department of Environmental Marine Sciences Division of Science and Technology Hanyang University) ;
  • Ju, Se-Jong (Marine Living Resource Research Department, KORDI) ;
  • Lee, Chang-Rae (Marine Living Resource Research Department, KORDI)
  • 고아라 (한양대학교 과학기술학부 해양환경과학과) ;
  • 주세종 (한국해양연구원 해양생물자원연구부) ;
  • 이창래 (한국해양연구원 해양생물자원연구부)
  • Published : 2009.03.30

Abstract

In an effort to better understand the physiological and ecological differences between warm and cold water copepod species in Korean waters using lipid contents and compositions, two species of copepods (Pleuromamma sp. as a warm water species and Neocalanus plumchrus as a cold water species) were collected from the Northwest Pacific and East Sea/Sea of Japan, respectively. The cold water species showed two fold higher lipid contents than the warm water species (11% vs. 5% of dry weight). Wax esters, known as one of the major storage lipid classes, were found to be the dominant lipid class (accounting for 64% of total lipids) in the cold water species, whereas, in the warm water species, phospholipids, which are known as membrane components, were the dominant lipid class (accounting for 43% of total lipids),with a trace amount of the storage lipids as a form of triacylglycerols (${\leq}1%$ of total lipids). With regard to the fatty acid compositions, saturated fatty acids (SAFA), especially 16:0 (about 30% of total fatty acids), were most abundant in the warm water species, whereas the polyunsaturated fatty acids (PUFA), particularly eicosapentaenoic acid (EPA : 20:5(n-3)) (${\geq}16%$ of total fatty acids), were most abundant in the cold water species. Among the neutral fraction of lipids, phytol, originating from the side chain of chlorophyll and indicative of active feeding on phytoplankton, was detected only in the warm water species. Significant quantities of fatty alcohols were detected in cold water species, particularly long-chain monounsaturated fatty alcohols (i.e. 20:1(n-9) and 22:1(n-11)), which are well known to abound in cold water herbivorous copepods. However, only trace amounts of short-chain fatty alcohols were detected in the warm water species. Twelve different kinds of sterols were detected in these copepod species, with cholest-5-en-$3{\beta}$-ol (cholesterol) and cholesta-5, 24-dien-$3{\beta}$-ol (desmosterol) dominating in cold and warm water species, respectively. In addition, for the warm water species (Pleuromamma sp.), we assessed the latitudinal gradients of lipid contents and compositions using samples from three different latitudinal regions (Philippine EEZ, Japan EEZ, and the East China Sea). Although no latitudinal gradients of lipid contents were detected, the lipid compositions, particularly dietary fatty acid markers, varied significantly with the latitude. The findings of this study confirm that the distribution of lipid contents and compositions in copepods may not only indicate their nutritional condition and diet history, but may also provide insights into their living strategies under different environmental conditions (i.e., water temperature, food availability).

Keywords

References

  1. 한국해양연구원 (2008) 북서 태평양이 한반도 주변해(대한해협)에 미치는 영향연구. 770 p
  2. Ackman RG (1989) Nutritional composition of fats in seafoods. Prog Food Nutr Sci 13:161-241
  3. Alvessard E, Mayzaud P (2003) Influence of the trophoclimatic environment and reproduction on the lipid composition of the euphausiid Meganyctiphanes norvegica from the Ligurian Sea, the Clyde Sea and the Kattegat. Mar Ecol Prog Ser 253:217-232 https://doi.org/10.3354/meps253217
  4. Auel H, Harjes M, da Rocha R, Stbing 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
  5. Barrett SM, Volkman JK, Dunstan GA (1995) Sterols of 14 species of marine diatoms (Baccillariophyta). J Phycol 31:360-369 https://doi.org/10.1111/j.0022-3646.1995.00360.x
  6. Batten SD, Welch DW, Jonas T (2003) Latitudinal differences in the duration of development of Neocalanus plumchrus copepodites. Fisheries Oceanogr 12:201-208 https://doi.org/10.1046/j.1365-2419.2003.00233.x
  7. Beaugrand G, Brander KM, Lindley JA, Souissi S, Reid PC (2002) Plankton effect on cod recruitment in the North Sea. Nature 426:661-664 https://doi.org/10.1038/nature02164
  8. Bennett JL, Hopkins TL (1989) Aspects of the ecology of the calanoid copepod genus Pleuromamma in the eastern Gulf of Mexico. Contributions in Mar Sci 31:119-136
  9. Benson AA, Lee RF (1975) The role of wax in oceanic food chains. Sci Am 232:77-83 https://doi.org/10.1038/scientificamerican0375-76
  10. 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
  11. Bottino NR (1974) The fatty acids of Antarctic phytoplankton and euphausiids. Fatty acid exchange among trophic levels of the Ross Sea. Mar Biol 27:197-204 https://doi.org/10.1007/BF00391944
  12. Bougis P (1976) Marine Plankton Ecology. Elsevier, New York, 169 p
  13. Budge SM, Springer AM, Iverson SJ, Sheffield G, Rosa C(2008) Blubber fatty acid composition of bowhead whales, Balaena mysticetus: Implication for diet assessment and ecosystem monitoring. J Exp Mar Biol Ecol 359:40-46
  14. Budge SM, Parrish CC (1998) Lipid biogeochemistry of plankton, settling matter and sediments in Trinity Bay, Newfoundland. II. Fatty acids. Organic Geochem 29:1547-1559 https://doi.org/10.1016/S0146-6380(98)00177-6
  15. Cripps GC, Watkins JL, Hill HJ, Atkinson A (1999) Fatty aicds content of Antarctic krill Euphausia superba at South Georgia related to regional populations and variations in diet. Mar Ecol Prog Ser 181:177-188 https://doi.org/10.3354/meps181177
  16. Cripps GC, Atkinson A (2000) Fatty acid composition as an indicator of carnivory in Antarctic krill, Euphausia superba. Canadian J Fish Aqua Sci 57:31-37 https://doi.org/10.1139/cjfas-57-S3-31
  17. Dalsgaard J, St John M, Kattner G, Mller-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
  18. 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
  19. 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
  20. 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 Biol 156:225-237 https://doi.org/10.1007/s00227-008-1073-1
  21. Evanson M, Bornhold EA, Goldblatt RH, Harrison PJ, Lewis AG (2000) Temporal variation in body composition and lipid storage of the overwintering, subarctic copepod Neocalanus plumchrus in the Strait of Georgia, British Columbia(Canada). Mar Ecol Prog Ser 192:239-247 https://doi.org/10.3354/meps192239
  22. Falk-Petersen S, Hagen W, Kattner G, Clarke A, Sargent J (2000) Lipids, trophic relationships, and biodiversity in Arctic and Antarctic krill. Canadian J Fish Aqua Sci 57:178-191 https://doi.org/10.1139/cjfas-57-S3-178
  23. Falk-Petersen S, Hopkins CCE, Sargent JR (1990) Trophic relationships in the pelagic, Arctic food web. In: Barnes M, Gibson RN (eds) Trophic relationships in marine environments. Proceedings of the 24th European marine biology symposium, Oban, Scotland, pp 315-333
  24. Falk-Petersen S, Sargent JR, Tande KS (1987) Lipid composition of zooplankton in relation to the sub-Arctic food web. Polar Biol 8:115-120 https://doi.org/10.1007/BF00297065
  25. 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
  26. 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 https://doi.org/10.1016/0198-0149(83)90029-8
  27. 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
  28. 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
  29. Graeve M, Kattner G, Piepenburg D (1997) Lipids in Arctic benthos: Does the fatty acid and alcohol composition reflect feeding and trophic interactions? Polar Biol 18: 53-61 https://doi.org/10.1007/s003000050158
  30. 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
  31. Hagen W, Auel H (2001) Seasonal adaptations and the role of lipids in oceanic zooplankton. Zoology 104:313-326 https://doi.org/10.1078/0944-2006-00037
  32. Hiroaki S, Yuichi K (2000) Lipids of four boreal species of calanoid copepods: Origin of monoene fats of marine animals at higher trophic levels in the grazing food chain in the subarctic ocean ecosystem. Mar Chem 71:69-82 https://doi.org/10.1016/S0304-4203(00)00041-4
  33. Ikeda T (1974) Nutritional ecology of marine zooplankton. Mem Fac Fish Hokkaido Univ 22:1-97
  34. Ju SJ, Harvey HR (2004) Lipids as markers of nutritional condition and diet in the Antarctic krill Euphausia superba and Euphausia crystallorophias during austral winter. Deep-Sea Res II 51:2199-2214 https://doi.org/10.1016/j.dsr2.2004.08.004
  35. Ju SJ, 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
  36. Ju SJ, Scolardi K, Daly KL, Harvey HR (2004) Understanding the trophic role of the Antarctic ctenophore, Callianira antarctica, using lipid boimarkers. Polar Biol 27:782-792 https://doi.org/10.1007/s00300-004-0652-y
  37. Kaneda T (1991) Iso- and anteiso-fatty acids in bacteria : biosynthesis, function, and taxonominc significance. Microbiol Rev 55(2):288-302
  38. 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
  39. Kattner G, Hagen W (1995) Polar herbivorous copepods - different pathways in lipid biosynthesis. ICES J Mar Sci 52:329-335 https://doi.org/10.1016/1054-3139(95)80048-4
  40. Kattner G, Brockmann UH (1990) Particulate and dissolved fatty acids in an enclosure containing a unialgal Skeletonema costatum (Greve) Cleve culture. J Exp Mar Biol Ecol 141:1-13 https://doi.org/10.1016/0022-0981(90)90153-4
  41. Lee RF, Nevenzel JC, Paffenhfer GA (1970) Wax esters in marine copepods. Sci 167:1510-1511 https://doi.org/10.1126/science.167.3924.1510
  42. 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
  43. Lee RF, Hirota J (1973) Wax esters in tropical zooplankton and nekton and the geographical distribution of wax esters in marine copepods. Limnol Oceanogr 18(2): 227-239 https://doi.org/10.4319/lo.1973.18.2.0227
  44. Littlepage JL (1964) Seasonal variation in lipid content of two Antarctic marine crustacean. In: Carrick R, Holdgate M, Prevost J (eds) Biologie antarctique. Hermann, Paris, pp 463-479
  45. Liu H, Hopcroft RR (2006) Growth and development of Neocalanus flemingeri/plumchrus in the northern Gulf of Alaska: validation of the artificial-cohort method in cold waters. J Plankton Res 28:87-101 https://doi.org/10.1093/plankt/fbi102
  46. Mayzaud P, Claustre H, Augier P (1990) Effect of variable nutrient supply on fatty acid composition of phytoplankton growth in an enclosed experimental ecosystem. Mar Ecol Prog Ser 60:123-140 https://doi.org/10.3354/meps060123
  47. 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
  48. Miller CB (1993) Development of large copepods during spring in the Gulf of Alaska. Prog Oceanogr 32:295-317 https://doi.org/10.1016/0079-6611(93)90018-9
  49. Morris RJ, McCartney MJ, Joint IR, Robinson HA (1985) Further studies of a spring phytoplankton bloom in an enclosed experimental ecosystem. Mar Ecol Prog Ser 86:151-170
  50. Nichols DS, Nichols PD, Sullivan CW (1993) Fatty acid, sterol and hydrocarbon composition of Antarctic Sea ice diatom communities during spring bloom in McMurdo Sound. Antarctic Sci 5(3):271-278 https://doi.org/10.1017/S0954102093000367
  51. Ohman MD (1996) Freezing and storage of copepod samples for the analysis of lipids. Mar Ecol Prog Ser 130:295-298 https://doi.org/10.3354/meps130295
  52. Pond DW, Sargent JR (1998) Lipid composition of the pelagic tunicate Dolioletta gegenbauri (Tunicata, Thaliacea). J Plankton Res 20:169-174 https://doi.org/10.1093/plankt/20.1.169
  53. Raymont JEG (1983) Plankton and productivity in the oceans, vol 2, zooplankton. Pergamon Press, Oxford, 824 p
  54. Roemmich D, McGowan J (1995) Sampling zooplankton:correction. Science 268:352-353 https://doi.org/10.1126/science.268.5209.352-b
  55. Sargent JR (1976) The structure, metabolism and function of lipids in marine organisms. Biochemical and biophysical perspectives in Mar Biol 3:150-212
  56. Sargent JR (1978) Marine wax esters. Sci Prog 65:437-457
  57. Sargent JR, Henderson J, Tocher DR (1989) The lipids. In:Halver, JE (ed) Fish nutrition. Academic Press, San Diego, pp 153-218
  58. Sargent JR, Falk-Petersen S (1981) Ecological investigations on the zooplankton community in Balsfjorden, Northern Norway : lipids and fatty acids in Meganyctiphanes norvegica, Thysanoessa raschi and T. inermis during mid-winter. Mar Biol 62:131-137 https://doi.org/10.1007/BF00388175
  59. Sargent JR, Falk-Petersen S (1988) The lipid biochemistry of calanoid copepods. Hydrobiologia 167/168:101-114 https://doi.org/10.1007/BF00026297
  60. Sargent JR, Henderson RJ (1986) Lipids. In: Corner EDS, O'Hara SCM (eds) The biological chemistry of marine copepods, vol 1. Clarendon Press, London, pp 59-108
  61. 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
  62. Virtue P, Nichols PD, Nicol S, McMinn A, Sikes EL (1993) The lipid composition of Euphausia superba Dana in relation to the nutritional value of Phaeocystis pouchetii (Hariot) Lagerheim. Antarctic Sci 5:169-177 https://doi.org/10.1017/S0954102093000239
  63. Volkman JK, Barrett SM, Blackburn SI, Mansour MP, Sikes EL, Gelin F (1998) Microalgal biomarkers: a review of recent research developments. Geochem 29:1163-1179 https://doi.org/10.1016/S0146-6380(98)00062-X
  64. Wimpenny RS (1966) The Plankton of the sea. Faber and Faber Ltd, London, 426 p

Cited by

  1. Physiological improvement in the copepodEurytemora affinisthrough thermal and multi-generational selection vol.47, pp.7, 2016, https://doi.org/10.1111/are.12675
  2. Spatial and temporal variations of the trophodynamics of anchovy (Engraulis japonicus) in the southern coastal waters of Korea using fatty acid trophic markers vol.18, pp.6, 2014, https://doi.org/10.1080/19768354.2014.982706
  3. Biomass and trophic structure of the plankton community in subtropical and temperate waters of the northwestern Pacific Ocean vol.68, pp.3, 2012, https://doi.org/10.1007/s10872-012-0111-2