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The Lipid Composition of the Coccolithophore Emiliania Huxleyi and Its Possible Ecophysiological Significance

Published online by Cambridge University Press:  11 May 2009

D.W. Pond
Affiliation:
Plymouth Marine Laboratory, Prospect Place, Plymouth, PL1 3DH
R.P. Harris
Affiliation:
Plymouth Marine Laboratory, Prospect Place, Plymouth, PL1 3DH

Extract

The lipid class and fatty acid composition of eight geographically disperse isolates of Emiliania huxleyi, grown under 12 h L:D cycles and harvested during logarithmic and stationary growth phases, were examined. Cell size and chlorophyll content tended to decrease from logarithmic to stationary growth phase, Methyl and ethyl ketones were the dominant lipid classes, although proportions exhibited no clear pattern either between strains or growth phases. Neutral lipid hardly accumulated over the course of the growth experiments, and triacylglycerol was either absent or only present at low levels. In all strains with the exception of a South African isolate, levels of total fatty acid per cell decreased markedly between logarithmic and stationary phases, primarily attributable to reductions in the levels of saturated and monounsaturated fatty acids. Major fatty acids in all strains during both growth phases were 14:0,16:0,18:1 (n-9), 18:4 (n-3), 18:5 (n-3) and 22:6 (n-3). Although all strains were rich in polyunsaturated fatty acids (47–72% of total fatty acids) stationary phase cultures consistently contained the highest proportions. The polyunsaturated fatty acid docosahexanoic acid (22:6, n-3) was the most abundant fatty acid in all strains, comprising a maximum of 38·4% of total fatty acids in strain M 181 during stationary phase. Multivariate analysis (PCA) allowed logarithmic and stationary phase cultures to be distinguished although no obvious intra-isolate variability was apparent. The results are discussed in terms of the importance of lipids for the ecophysiology of E. huxleyi and the role of this dominant coccolithophore in the marine food chain.

Type
Research Article
Copyright
Copyright © Marine Biological Association of the United Kingdom 1996

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References

Anderson, O.R., Spindler, M., , A.W.H. & Hemleben, C.H., 1979. Trophic activity of planktonic foraminifera. Journal of the Marine Biological Association of the United Kingdom, 59, 791799.CrossRefGoogle Scholar
Bell, M.V. & Dick, J.R., 1993. The appearance of rods in the eyes of herring and increased didocosahexaenoyl molecular species of phospholipids. Journal of the Marine Biological Association of the United Kingdom, 73, 679688.Google Scholar
Blumer, M., Mullin, M.M. & Thomas, D.W., 1964. Pristane in the marine environment. Helgoländer Wissenschaftliche Meeresuntersuchungen, 10, 187201.Google Scholar
Brand, L.E., 1982. Genetic variability and spatial patterns of genetic differentiation in the reproductive rates of the marine coccolithophores Emiliania huxleyi and Gephyrocapsa oceanica. Limnology and Oceanography, 27, 236245.CrossRefGoogle Scholar
Christie, W.W., 1982. Lipid analyses, 2nd Ed.Oxford: Pergamon Press, [pp. 5253.]Google Scholar
Chuecas, L. & Riley, J.P., 1969. Component fatty acids of the total lipids of some marine phytoplankton. Journal of the Marine Biological Association of the United Kingdom, 49, 97116.Google Scholar
Conte, M.H. & Eglinton G., 1993. Alkenone and alkenoate distributions within the euphotic zone of the eastern North Atlantic: correlation with production temperature. Deep-Sea Research, 40, 19351961.Google Scholar
Conte, M.H., Eglinton, G. & Madureria, L.A.S., 1992. Long-chain alkenones and alkyl alkenoates as paleotemperature indicators: their production flux and early sedimentary diagenesis in the eastern North Atlantic. In Advances in organic geochemistry 1991 (ed. C.B., Eckardtet al.), pp. 287298. Oxford: Pergamon Press. [Organic Geochemistry, 19.]Google Scholar
Conte, M.H., Thompson, A. & Eglinton, G., 1994 a. Primary production of biomarker compounds by Emiliania huxleyi: results from an experimental mesocosm study in the fjords of south-western Norway. Sarsia, 79, 319332.Google Scholar
Conte, M.H., Thompson, A., Eglinton, G. & Green, J.C., 1995. Lipid biomarker diversity in the coccolithophorid Emiliania huxleyi (Prymnesiophycae) and the related species Gephyrocapsa oceanica. Journal ofPhycology, 31, 272282.Google Scholar
Conte, M.H., Volkman, J.K. & Eglinton, G., 1994 b. Lipid biomarkers of the Haptophyta. In The biology of the Haptophyta algae (ed. J.C., Green and B.L., Leadbetter), pp 351378. Oxford: Claredon Press. [Systematics Association, special vol. no. 51.]CrossRefGoogle Scholar
Delaunay, F., Marty, Y., Moal, J. & Samain, J.-E., 1993. The effect of monospecific algal diets on growth and fatty acid composition of Pecten maximus (L.) larvae. Journal of Experimental Marine Biology and Ecology, 173, 163179.Google Scholar
Fernandez, E., Balch, W.M., Maranon, E. & Holligan, P., 1994. High rates of lipid biosynthesis in cultured, mesocosm and coastal populations of the coccolithophorid Emiliania huxleyi. Marine Ecology Progress Series, 114, 1322.Google Scholar
Fernandez, E., Boyd, P., Holligan, P.M. & Harbour, D.S., 1993. Production of organic and inorganic carbon within a large-scale coccolithophore bloom in the north-east Atlantic Ocean. Marine Ecology Progress Series, 97, 271285.Google Scholar
Folch, J., Lees, M. & Sloan, 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
Guillard, R.R.L. & Ryther, J.H., 1962. Studies of marine planktonic diatoms. I. Cyclotella nana Hustedt, and Detonula confervacea (Cleve) Gran. Canadian Journal of Microbiology, 8, 229239.Google Scholar
Harris, R.P., 1994. Zooplankton grazing on the coccolithophore Emiliania huxleyi and its role in inorganic carbon flux. Marine Biology, 119, 431439.Google Scholar
Harwood, J.L. & Russell, N.J., 1984. Lipids in plants and microbes. London: Allen & Unwin.Google Scholar
Hodgson, P., Henderson, R.J., Sargent, J.R. & Leftley, J.W., 1991. Patterns of variation in the lipid class and fatty acid composition of Nannochloropsis oculata (Eustigmatophyceae) during batch culture. I. The growth cycle. Journal of Applied Phycology, 3, 169181.Google Scholar
Holligan, P.M. & Groom, S.B., 1986. Phytoplankton distributions along the shelf break. Proceedings of the Royal Society of Edinburgh B, 88, 239263.Google Scholar
Holligan, et al., 1993. A biogeochemical study of the coccolithophore, Emiliania huxleyi in the North Atlantic. Global Biogeochemical Cycles, 7, 879900.Google Scholar
Hori, T. & Green, J.C., 1985. An ultrastructural study of mitosis in non-motile coccolith-bearing cells of Emiliania huxleyi (Lohm.) Hay & Mohler (Prymnesiophycae). Protistologica, 21, 107120.Google Scholar
Huntley, M.E., Ciminiello, P. & Lopez, M.D.G., 1987. Importance of food quality in determining development and survival of Calanus pacificus (Copepoda: Calanoida). Marine Biology, 95, 103113.Google Scholar
Jónasdóttir, S. H., 1994. Effects of food quality on the reproductive success of Acartia tonsa and Acartia hudsonica: laboratory observations. Marine Biology, 121, 6781.CrossRefGoogle Scholar
Jordan, R., Winter, A. & Roth P., 1994. Biogeography of living coccolithophorids in ocean waters. In Coccolithophores (ed. A., Winter and W.G., Seisser), pp. 161178. Cambridge University Press.Google Scholar
Kanazawa, A., Teshima, S. & Ono, K., 1979. Relationship between essential fatty acid requirements of aquatic animals and their capacity for bioconversion of linolenic acid to highly unsaturated fatty acids. Comparative Biochemistry and Physiology, 63B, 295298.Google ScholarPubMed
Kuenzler, E.J. & Perras, J.P., 1965. Phosphatases of marine algae. Biological Bulletin. Marine Biological Laboratory, Woods Hole, 128, 271284.CrossRefGoogle Scholar
Lancelot, C. & Mathot, S., 1987. Dynamics of a Phaeocystis-dominated spring bloom in Belgian coastal waters. I. Phytoplankton activities and related parameters. Marine Ecology Progress Series, 37, 239248.Google Scholar
Langdon, C.J. & Waldock, M.J., 1981. The effect of algal and artificial diets on the growth and fatty acid composition of Crassostrea gigas spat. Journal of the Marine Biological Association of the United Kingdom, 61, 431448.Google Scholar
Lee, R.F. & Loeblich, A.R., 1971. Distribution of 21:6 hydrocarbon and its relationship to 22:6 fatty acid in algae. Photochemistry, 10, 593602.CrossRefGoogle Scholar
Lewis, R.W., 1970. The densities of three classes of marine lipids in relation to their possible roles as hydrostatic agents. Lipids, 5, 151153.Google Scholar
Marlowe, I.T., 1984. Lipids as paleoclimatic indicators. PhD thesis, University of Bristol.Google Scholar
Marlowe, I.T., Green, J.C., Neal, A.C., Brassell, S.C., Eglinton, G. & Course, P.A., 1984. Long chain (n-C37-C39) alkenones in the Prymnesiophyceae. Distribution of alkenones and other lipids and their taxonomic significance. Journal of Phycology, 19, 203216.Google Scholar
Newcombe, A.G. & Reid, S.G., 1953. Chromatographic separation, using chemically treated paper, of aldehydes and ketones on the basis of their reactivity. Nature, London, 153, 455456.CrossRefGoogle Scholar
Okada, H. & Mclntyre, A., 1977. Modern coccolithophores of the Pacific and North Atlantic Ocean. Micropaleontology, 23, 155.Google Scholar
Okuyama, H., Kogame, K. & Takeda, S., 1993. Phylogenic significance of the limited distribution of octadecapentaenoic acid in prymnesiophytes and photosynthetic dinoflagellates. Proceedings NIPR Symposium Polar Biology, 6, 2126.Google Scholar
Olsen, R.E. & Henderson, R.J., 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.Google Scholar
Palmisano, A.C., Soohoo, J.B., Soohoo, S.L., Kottmeier, S.T., Craft, L.L. & Sullivan, C.W., 1986. Photoadaptation of Phaeocystis pouchetii advected beneath annual sea ice in McMurdo Sound, Antarctica. Journal of Plankton Research, 8, 891906.Google Scholar
Parrish, C.C. & Wangersky, P.J., 1987. Particulate and dissolved lipid classes in cultures of Phaeodactylum tricornutum grown in cage turbidistats with a range of nitrogen supply rates. Marine Ecology Progress Series, 35, 119128.Google Scholar
Pond, D.W., Priddle, J., Sargent, J.R. & Watkins, J.L., 1993. Lipid content and composition of Antarctic microplankton in relation to the nutrition of krill. Proceedings of British Antarctic Survey Special Topic Award Scheme Symposium, 30 September-1 October, 133139.Google Scholar
Pond, D.W., Priddle, J., Sargent, J.R. & Watkins J.L., 1993. Lipid content and composition of Antarctic microplankton in relation to the nutrition of krill. In University research in Antarctica, 1989–1992 (ed. R.B., Haywood), pp. 133139. Cambridge: British Antarctic Survey.Google Scholar
Pond, D.W., Priddle, J., Sargent, J.R. & Watkins J.L., 1994. Laboratory studies of assimilation and egestion of algal lipid by Antarctic krill - methods and initial results. Journal of Experimental Marine Biology and Ecology, 187, 253268.Google Scholar
Rechka, J.A. & Maxwell, J.R., 1988. Characterisation of alkenone temperature indicators in sediments and organisms. In Advances in organic geochemistry 1987 (ed. L., Mattavelli and L., Novelli), pp. 727734. [Organic Geochemistry, 13.]Google Scholar
Ryan, B.F., Joiner, B.L. & Ryan, T.A., 1988. MINITAB statistical package software. Reference manual release 8.1. Boston: PWS Publishers.Google Scholar
Sargent, J.R., Henderson, R.J. & Tocher, D.R., 1989. The lipids. In Fish nutrition (ed. J.E., Halver), pp 153218. New York: Academic Press.Google Scholar
Schofield, O., Bidigare, R.R. & Prézelin, B.B., 1990. Spectral photosynthesis, quantum yield and blue-green light enhancement of productivity rates in the diatom Chaetoceros gradate and the prymnesiophyte Emiliania huxleyi. Marine Ecology Progress Series, 64, 175186.CrossRefGoogle Scholar
Strickland, J.D.H. & Parsons, T.R., 1972. A practical handbook of sea-water analysis. Bulletin of the Fisheries Research Board of Canada, 310 pp.Google Scholar
Tinoco, J., 1982. Dietary requirements and functions of a-linolenic acid in animals. Progress in Lipid Research, 21, 145.Google Scholar
Verity, P.G. & Smayda, T.J., 1989. Nutritional value of Phaeocystis pouchetii (Prymnesiophyceae) and other phytoplankton for Acartia spp. (Copepoda): ingestion, egg production, and growth of nauplii. Marine Biology, 100, 161171.Google Scholar
Verity, P.G., Villareal, T. A. & Smayda. T.J., 1988. Ecological investigations of blooms of colonial Phaeocystis pouchetti. II. The role of life-cycle phenomena in bloom termination. Journal of Plankton Research, 10, 749766.CrossRefGoogle Scholar
Virtue, P., Nichols, P.D., Nichol, S., McMinn, A. & Sykes, E.L., 1993. The lipid composition of Euphausia superba Dana in relation to the nutritional value of Phaeocystis pouchetii (Hariot) Lagerheim. Antarctic Science, 5, 169177.Google Scholar
Volkman, J.K., Eglinton, E.D.S. & Sargent J.R., 1980. Long-chain alkenes and alkenones in the marine coccolithophorid Emiliania huxleyi. Phytochemistry, 19, 26192622.Google Scholar
Volkman, J.K., Jeffrey, S.W., Nichols, P.D., Rogers, G.I. & Garland, C.D., 1989. Fatty acid and lipid composition of ten species of microalgae used in mariculture. Journal of Experimental Marine Biology and Ecology, 128, 219240.CrossRefGoogle Scholar
Volkman, J.K., Smith, D.J., Eglinton, G., Foresberg, T.E.V. & Corner, E.D.S., 1981. Sterol and fatty acid composition of four marine Haptophycean algae. Journal of the Marine Biological Association of the United Kingdom, 61, 509527.Google Scholar
Westbrook, et al., 1994. A model system approach to biological climate forcing. The example of Emiliania huxleyi. Global and Planetary Change, 8, 2746.Google Scholar
Williams, R. & Lindley, J.A., 1980. Plankton of the Fladen Ground during FLEX 76 III. Vertical distribution, population dynamics and production of Calanus finmarchicus (Crustacea: Copepoda). Marine Biology, 60, 4756.Google Scholar
Yentsch, C.S. & Menzel, D.W., 1963. A method for the determination of phytoplankton chlorophyll and phaeophytin by fluorescence. Deep-Sea Research, 10, 221231.Google Scholar