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Dynamics of blood chylomicron fatty acids in a marine carnivore: implications for lipid metabolism and quantitative estimation of predator diets

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Abstract

Blubber fatty acid(s) (FA) signatures can provide accurate estimates of predator diets using quantitative FA signature analysis, provided that aspects of predator FA metabolism are taken into account. Because the intestinal absorption of dietary FA and their incorporation into chylomicrons (the primary transport lipoproteins for dietary FA in the blood) may influence the relationship between FA composition in the diet and adipose tissue, we investigated the metabolism of individual FA at these early stages of assimilation. We also investigated the capacity of chylomicron signatures to provide quantitative estimates of prey composition of an experimental meal. Six captive juvenile grey seals (Halichoerus grypus) were fed either 2.3 kg (n=3) or 4.6 kg (n=3) of Atlantic herring (Clupea harengus). Although chylomicron FA signatures resembled diet signatures at all samplings, absolute differences were smallest at 3-h post-feeding, when chylomicrons were likely largest and had the greatest ratio of triacylglycerol to phospholipid FA. Specific FA that differed significantly between diet and chylomicron signatures reflected either input from endogenous sources or loss through peroxisomal β-oxidation. When these aspects of metabolism were accounted for, the quantitative predictions of diet composition generated using chylomicron signatures were extremely accurate, even when tested against 28 other prey items.

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Abbreviations

FA:

Fatty acid(s)

FAME:

Fatty acid methyl ester(s)

K-L:

Kulback-Leibler

MUFA:

Monounsaturated fatty acid(s)

PL:

Phospholipid(s)

PUFA:

Polyunsaturated fatty acid(s)

QFASA:

Quantitative fatty acid signature analysis

SFA:

Saturated fatty acid(s)

TAG:

Triacylglycerol(s)

VLDL:

Very low-density lipoproteins

References

  • Becker C, Lund P, Hølmer G (2001) Effect of randomization of mixtures of butter oil and vegetable oil on absorption and lipid metabolism in rats. Eur J Nutr 40:1–9

    Google Scholar 

  • Bigg MA, Fawcett IF (1985) Two biases in diet determination of northern fur seals (Callorhinus ursinus). In: Beddington JR, Beverton RJH, Lavigne DM (eds) Marine mammals and fisheries. George Allen and Unwin, London, pp 284–291

    Google Scholar 

  • Boquillon M, Paris R, Clement J (1977) The effect of various dietary factors on the size distribution of lymph fat particles in the rat. Lipids 12:500–504

    Google Scholar 

  • Bowen WD (2000) Reconstruction of pinniped diets: accounting for complete digestion of otoliths and cephalopod beaks. Can J Fish Aquat Sci 57:898–905

    Article  Google Scholar 

  • Bremer J, Norum KR (1982) Metabolism of very long-chain monounsaturated fatty acids (22:1) and the adaptation to their presence in the diet. J Lipid Res 23:243–256

    Google Scholar 

  • Brindley DN (1991) Metabolism of triacylglycerols. In: Vance DE, Vance J (eds) Biochemistry of lipids, lipoproteins and membranes. Elsevier, Amsterdam, pp 171–203

    Google Scholar 

  • Budge SM, Iverson SJ, Bowen WD, Ackman RG (2002) Among and within species variability in fatty acid signatures of marine fish and invertebrates on the Scotian Shelf, Georges Bank, and southern Gulf of St Lawrence. Can J Fish Aquat Sci 59:886–898

    Article  Google Scholar 

  • Charnock JS, McLennan PL, Abeywardena MY, Russell GR (1985) Altered levels of n-6/n-3 fatty acids in rat heart and storage fat following variable dietary intake of linoleic acid. Annu Nutr Met 29:279–288

    Google Scholar 

  • Chen IS, Subramaniam S, Cassidy MM, Sheppard AJ, Vahouny GV (1985) Intestinal absorption and lipoprotein transport of (ω-3) eicosapentaenoic acid. J Nutr 115:219–225

    Google Scholar 

  • Christensen MS, Høy C-E (1996) Effects of dietary triacylglycerol structure on triacylglycerols of resultant chylomicrons from fish oil- and seal oil-fed rats. Lipids 31:341–344

    Google Scholar 

  • Christiansen RZ, Christiansen EN, Bremer J (1979) The stimulation of erucate metabolism in isolated rat hepatocytes by rapeseed oil and hydrogenated marine oil-containing diets. Biochim Biophys Acta 573:417–429

    Google Scholar 

  • Cook HW (1991) Fatty acid desaturation and chain elongation in eucaryotes. In: Vance DE, Vance J (eds) Biochemistry of lipids, lipoproteins and membranes. Elsevier, Amsterdam, pp 141–169

    Google Scholar 

  • Cooper MH (2004) Fatty acid metabolism in marine carnivores: implications for quantitative estimation of predator diets. PhD Thesis. Dalhousie University, Halifax

    Google Scholar 

  • Dahl TM, Lydersen C, Kovacs KM, Falk-Petersen S, Sargent J, Gjertz I, Gulliksen B (2000) Fatty acid composition of the blubber in white whales (Delphinapterus leucas). Polar Biol 23:401–409

    Article  Google Scholar 

  • Davis RA (1991) Lipoprotein structure and secretion. In: Vance DE, Vance J (eds) Biochemistry of lipids, lipoproteins and membranes. Elsevier, Amsterdam, pp 403–426

    Google Scholar 

  • Dellinger T, Trillmich F (1988) Estimating diet composition from scat analysis in otariid seals (Otariidae): is it reliable? Can J Zool 66:1865–1870

    Google Scholar 

  • Ekström B, Nilsson Å, Å kesson B (1989) Lipolysis of polyenoic fatty acid esters of human chylomicrons by lipoprotein lipase. Eur J Clin Invest 19:259–264

    Google Scholar 

  • Emken EA, Adlof RO, Rohwedder WK, Gulley RM (1993) Influence of linoleic acid on desaturation and uptake of deuterium-labeled palmitic and stearic acids in humans. Biochim Biophys Acta 1170:173–181

    Google Scholar 

  • Fielding BA, Samra JS, Ravell CL, Frayn KN (1999) Metabolism of individual fatty acids during infusion of a triacylglycerol emulsion. Lipids 34:535–541

    Google Scholar 

  • Folch J, Lees M, Stanley GHS (1957) A simple method for the isolation and purification of total lipides from animal tissues. J Biol Chem 226:497–509

    CAS  PubMed  Google Scholar 

  • Fraser R, Cliff WJ, Courtice FC (1968) The effect of dietary fat load on the size and composition of chylomicrons in thoracic duct lymph. Q J Exp Physiol 53:390–398

    Google Scholar 

  • Gangl A, Ockner RK (1975) Intestinal metabolism of plasma free fatty acids. Intracellular compartmentation and mechanisms of control. J Clin Invest 55:803–813

    Google Scholar 

  • Gangl A, Renner F (1978) In vivo metabolism of plasma free fatty acids by intestinal mucosa of man. Gastroenterology 74:847–850

    Google Scholar 

  • Gibney MJ, Daly E (1994) The incorporation of n-3 polyunsaturated fatty acids into plasma lipid and lipoprotein fractions in the postprandial phase in healthy volunteers. Eur J Clin Nutr 48:866–872

    Google Scholar 

  • Griffiths AJ, Humphreys SM, Clark ML, Fielding BA, Frayn KN (1994) Immediate metabolic availability of dietary fat in combination with carbohydrate. Am J Clin Nutr 59:53–59

    CAS  PubMed  Google Scholar 

  • Hansen J-B, Grimsgaard S, Nilsen H, Nordøy A, Bønaa KH (1998) Effects of highly purified eicosapentaenoic acid and docosahexaenoic acid on fatty acid absorption, incorporation into serum phospholipids and postprandial triglyceridemia. Lipids 33:131–138

    Google Scholar 

  • Harris WS, Connor WE, Alam N, Illingworth DR (1988) Reduction of postprandial triglyceridemia in humans by dietary n-3 fatty acids. J Lipid Res 29:1451–1460

    Google Scholar 

  • Hayashi H, Fujimoto K, Cardelli JA, Nutting DF, Bergstedt S, Tso P (1990) Fat feeding increases size, but not number, of chylomicrons produced by small intestine. Am J Physiol 259:G709–G719

    Google Scholar 

  • Hopkins MJ, Sharp R, Macfarlane GT (2001) Age and disease related changes in intestinal bacterial populations assessed by cell culture, 16S rRNA abundance, and community cellular fatty acid profiles. Gut 48:198–205

    Article  Google Scholar 

  • Iverson SJ (1988) Composition, intake and gastric digestion of milk lipids in pinnipeds. Thesis, University of Maryland, College Park

  • Iverson SJ (1993) Milk secretion in marine mammals in relation to foraging: can milk fatty acids predict diet? Symp Zool Soc Lond 66:263–291

    Google Scholar 

  • Iverson SJ, Sampugna J, Oftedal OT (1992) Positional specificity of gastric hydrolysis of long-chain n-3 polyunsaturated fatty acids of seal milk triglycerides. Lipids 27:870–878

    Google Scholar 

  • Iverson SJ, Arnould JPY, Boyd IL (1997a) Milk fatty acid signatures indicate both major and minor shifts in the diet of lactating Antarctic fur seals. Can J Zool 75:188–197

    Google Scholar 

  • Iverson SJ, Frost KJ, Lowry LF (1997b) Fatty acid signatures reveal fine scale structure of foraging distribution of harbor seals and their prey in Prince William Sound, Alaska. Mar Ecol Prog Ser 151:255–271

    Google Scholar 

  • Iverson SJ, Lang SLC, Cooper MH (2001) Comparison of the Bligh and Dyer and Folch methods for total lipid determination in a broad range of marine tissues. Lipids 36:1283–1287

    Google Scholar 

  • Iverson SJ, Frost KJ, Lang SLC (2002) Fat content and fatty acid composition of forage fish and invertebrates in Prince William Sound, Alaska: factors contributing to among and within species variability. Mar Ecol Prog Ser 241:161–181

    CAS  Google Scholar 

  • Iverson SJ, Field C, Bowen WD, Blanchard W (2004) Quantitative fatty acid signature analysis: a new method of estimating predator diets. Ecol Monogr 74(2):211–235

    Google Scholar 

  • Jobling M (1987) Marine mammal faecal samples as indicators of prey importance—a source of error in bioenergetics studies. Sarsia 72:255–260

    Google Scholar 

  • Jobling M, Breiby A (1986) The use and abuse of fish otoliths in studies of feeding habits of marine piscivores. Sarsia 71:265–274

    Google Scholar 

  • Käkelä R, Hyvarinen H, Vainiotalo P (1993) Fatty acid composition in liver and blubber of the Saimaa ringed seal (Phoca hispida saimensis) compared to that of the ringed seal (Phoca hispida botnica) and grey seal (Halichoerus grypus) from the Baltic. Comp Biochem Physiol B 105:553–565

    Article  Google Scholar 

  • Karmen A, Whyte M, Goodman DS (1963) Fatty acid esterification and chylomicron formation during fat absorption: 1. Triglycerides and cholesterol esters. J Lipid Res 4:312–321

    Google Scholar 

  • Kawamoto T, Okano G, Akino T (1980) Biosynthesis and turnover of individual molecular species of phosphatidylcholine in liver and bile. Biochim Biophys Acta 619:20–34

    Google Scholar 

  • Kayden HJ, Karmen A, Dumont A (1963) Alterations in the fatty acid composition of human lymph and serum lipoproteins by single feedings. J Clin Invest 42:1373–1381

    Google Scholar 

  • Kirsch PE, Iverson SJ, Bowen WD, Kerr SR, Ackman RG (1998) Dietary effects on the fatty acid signature of whole Atlantic cod (Gadus morhua). Can J Fish Aquat Sci 55:1378–1386

    Article  Google Scholar 

  • Kirsch PE, Iverson SJ, Bowen WD (2000) Effect of a low-fat diet on body composition and blubber fatty acids of captive juvenile harp seals (Phoca groenlandica). Physiol Biochem Zool 73:45–59

    Article  Google Scholar 

  • Kotz S, Johnson NLE (1983) The Kulback distance. In: The encyclopedia of statistics. Wiley, New York, USA, pp 421--425

  • Lai H-C, Ney DM (1998) Gastric digestion modifies absorption of butterfat into lymph chylomicrons in rats. J Nutr 128:2408–2410

    Google Scholar 

  • Lambert MS, Botham KM, Mayes PA (1996) Modification of the fatty acid composition of dietary oils and fats on incorporation into chylomicrons and chylomicron remnants. Brit J Nutr 76:435–445

    Google Scholar 

  • Levy R, Herzberg GR (1996) Effects of a meal of fish oil or corn oil on bile flow and composition in rats previously adapted to diets containing fish oil or corn oil. Nutr Res 16:805–816

    Article  Google Scholar 

  • Levy R, Herzberg GR (1999) Hydrolysis of long-chain, n-3 fatty acid enriched chylomicrons by cardiac lipoprotein lipase. Can J Physiol Pharmacol 77:813–818

    Article  Google Scholar 

  • Leyton J, Drury PJ, Crawford MA (1987) In vivo incorporation of labeled fatty acids in rat liver lipids after oral administration. Lipids 22:553–558

    Google Scholar 

  • Lhuillery C, Mebarki S, Lecourtier M-J, Demarne Y (1988) Influence of different dietary fats on the incorporation of exogenous fatty acids into rat adipose glycerides. J Nutr 118:1447–1454

    Google Scholar 

  • Luchoomun J, Hussain MM (1999) Assembly and secretion of chylomicrons by differentiated caco-2 cells: nascent triglycerides and preformed phospholipids are preferentially used for lipoprotein assembly. J Biol Chem 274:19565–19572

    Article  Google Scholar 

  • MacDonald JIS, Sprecher H (1991) Phospholipid fatty acid remodeling in mammalian cells. Biochim Biophys Acta 1084:105–121

    Google Scholar 

  • Mansbach CMI, Dowell RF (1992) Uptake and metabolism of circulating fatty acids by rat intestine. Am J Physiol 263:G927–G933

    Google Scholar 

  • Mansbach CMI, Dowell RF (1994) Intestine competes with liver for the uptake of chylomicron remnants in vivo. Gastroenterology 106:A620

    Google Scholar 

  • Mansbach CMI, Dowell RF (1995) Role of the intestine in chylomicron remnant clearance. Am J Physiol 269:G144–G152

    Google Scholar 

  • Mansbach CMI, Nevin P (1998) Intracellular movement of triacylglycerols in the intestine. J Lipid Res 39:963–968

    Google Scholar 

  • Mansbach CMI, Parthasarathy S (1982) A re-examination of the fate of glyceride-glycerol in neutral lipid absorption and transport. J Lipid Res 23:1009–1019

    Google Scholar 

  • Melin T, Qi C, Bengtsson-Olivecrona G, Å kesson B, Nilsson Å (1991) Hydrolysis of chylomicron polyenoic fatty acid esters with lipoprotein lipase and hepatic lipase. Biochim Biophys Acta 1075:259–266

    Google Scholar 

  • Melin T, Qi C, Nilsson Å (1996) Bile but not chyle lipoprotein is an important source of arachidonic acid for the rat small intestine. Prostaglandins Leukotrienes Essent Fatty Acids 55:337–343

    Article  Google Scholar 

  • Moore LVH, Bourne DM, Moore WEC (1994) Comparative distribution and taxonomic value of cellular fatty acids in thirty-three genera of anaerobic gram-negative bacteria. Int J Syst Bacteriol 44:338–347

    CAS  PubMed  Google Scholar 

  • Morrison WR, Smith LM (1964) Preparation of fatty acid methyl esters and dimethylacetals from lipids with boron fluoride-methanol. J Lipid Res 5:600–608

    CAS  Google Scholar 

  • Neat CE, Thomassen MS, Osmundsen H (1980) Induction of peroxisomal beta-oxidation in rat liver by high-fat diets. Biochem J 186:369–371

    Google Scholar 

  • Neat CE, Thomassen MS, Osmundsen H (1981) Effect of high-fat diets on hepatic fatty acid oxidation in the rat. Isolation of rat liver peroxisomes by vertical-rotor centrifugation by using a self-generated, iso-osmotic, Percoll gradient. Biochem J 196:149–159

    Google Scholar 

  • Nilsson Å, Landin B (1988) Metabolism of chylomicron arachidonic and linoleic acid in the rat. Biochim Biophys Acta 959:288–295

    Google Scholar 

  • Nilsson Å, Melin T (1988) Absorption and metabolism of orally fed arachidonic and linoleic acid in the rat. Am J Physiol 255:G612–G618

    Google Scholar 

  • Nilsson Å, Landin B, Jensen E, Å kesson B (1987a) Absorption and lymphatic transport of exogenous and endogenous arachidonic and linoleic acid in the rat. Am J Physiol 252:G817–G824

    Google Scholar 

  • Nilsson Å, Landin B, Schotz MC (1987b) Hydrolysis of chylomicron arachidonate and linoleate ester bonds by lipoprotein lipase and hepatic lipase. J Lipid Res 28:510–517

    Google Scholar 

  • Nilsson Å, Hjelte L, Strandvik B (1992) Incorporation of dietary [14 C]arachidonic acid and [3H]eicosapentaenoic acid into tissue lipids during absorption of a fish oil emulsion. J Lipid Res 33:1295–1305

    Google Scholar 

  • Noma A (1964) Studies on the phospholipid metabolism of the intestinal mucosa during fat absorption. J Biochem 56:522–532

    Google Scholar 

  • Novikoff PM, Novikoff AB (1972) Peroxisomes in absorptive cells of mammalian small intestine. J Cell Biol 53:532–560

    Article  Google Scholar 

  • Ockner RK, Hughes FB, Isselbacher KJ (1969) Very low density lipoproteins in intestinal lymph: role in triglyceride and cholesterol transport during fat absorption. J Clin Invest 48:2367–2373

    Google Scholar 

  • Ong J, Bexard J, Lecerf J (1977) Incorporation and metabolic conversion of erucic acid in various tissues of the rat in short term experiments. Lipids 12:563–569

    Google Scholar 

  • Osmundsen H, Neat CE, Norum KR (1979) Peroxisomal oxidation of long chain fatty acids. FEBS Lett 99:292–296

    Article  Google Scholar 

  • Patton GM, Bennett Clark S, Fasulo JM, Robins SJ (1984) Utilization of individual lecithins in intestinal lipoprotein formation in the rat. J Clin Invest 73:231–240

    Google Scholar 

  • Pelech SL, Vance DE (1984) Regulation of phosphotidylcholine biosynthesis. Biochim Biophys Acta 779:217–251

    Google Scholar 

  • Perez JA, Rodriguez C, Henderson RJ (1999) The uptake and esterification of radiolabelled fatty acids by enterocytes isolated from rainbow trout (Oncorhynchus mykiss). Fish Physiol Biochem 20:125–134

    Article  Google Scholar 

  • Poulos A, Sharp P, Fellenberg AJ, Johnson DW (1988) Accumulation of pristanic acid (2,6,10,14-tetramethylpentadecanoic acid) in plasma of patients with generalized peroxisomal dysfunction. Eur J Pediatr 147:143–147

    Article  Google Scholar 

  • Raclot T, Groscolas R, Cherel Y (1998) Fatty acid evidence for the importance of myctophid fishes in the diet of king penguins, Aptenodytes patagonicus. Mar Biol 132:523–533

    Article  Google Scholar 

  • Redgrave TG (1983) Formation and metabolism of chylomicrons. Int Rev Physiol 28:103–130

    Google Scholar 

  • Redgrave TG, Dunne KB (1975) Chylomicron formation and composition in unanaesthetised rabbits. Atherosclerosis 22:389–400

    Google Scholar 

  • Ridgway N, Dolphin PJ (1984) Lipoprotein lipase-mediated sequestration of long chain polyunsaturated triacylglycerols in serum LDL from normal and hypothyroid rats. Biochim Biophys Acta 796:64–71

    Google Scholar 

  • Roshanai F, Sanders TAB (1985) Influence of different supplements of n-3 polyunsaturated fatty acids on blood and tissue lipids in rats receiving high intakes of linoleic acid. Annu Nutr Met 29:189–196

    Google Scholar 

  • Rouvinen K, Kiiskinen T (1989) Influence of dietary fat source on the body fat composition of mink (Mustela vison) and blue fox (Alopex lagopus). Acta Agric Scand 39:279–288

    Google Scholar 

  • Sakr SW, Attia N, Haouringui M, Paul JL, Soni T, Vacher D, Girard-Globa A (1997) Fatty acid composition of an oral load affects chylomicron size in human subjects. Br J Nutr 77:19–31

    Google Scholar 

  • Schacky C von, Weber PC (1985) Metabolism and effects on platelet function of the purified eicosapentaenoic and docosahexaenoic acids in humans. J Clin Invest 76:2446–2450

    Google Scholar 

  • Schwalme K (1992) A quantitative comparison between diet and body fatty acid composition in wild northern pike (Esox lucius L.). Fish Physiol Biochem 10:91–98

    Article  Google Scholar 

  • Sheehe DM, Green JB, Green MH (1980) Influence of dietary fat saturation on lipid absorption in the rat. Atherosclerosis 37:301–310

    Google Scholar 

  • Shiau Y-F, Popper DA, Reed M, Umstetter C, Capuzzi D, Levine GM (1985) Intestinal triglycerides are derived from both endogenous and exogenous sources. Am J Physiol 248:G164–G169

    Google Scholar 

  • Shrivastava BK, Redgrave TG, Simmonds WJ (1967) The source of endogenous lipid in the thoracic duct lymph of fasting rats. Q J Exp Physiol 52:305–312

    Google Scholar 

  • da Silva J, Neilson JD (1985) Limitation of using otoliths recovered in scats to estimate prey consumption in seals. Can J Fish Aquat Sci 42:1439–1442

    Google Scholar 

  • Singh H, Brogan M, Johnson D, Poulos A (1992) Peroxisomal ß-oxidation of branched chain fatty acids in human skin fibroblasts. J Lipid Res 33:1597–1605

    Google Scholar 

  • Smith RJ, Hobson KA, Koopman HN, Lavigne DM (1996) Distinguishing between populations of fresh- and salt-water harbour seals (Phoca vitulina) using stable-isotope ratios and fatty acid profiles. Can J Fish Aquat Sci 53:272–279

    Article  Google Scholar 

  • Smith SJ, Iverson SJ, Bowen WD (1997) Fatty acid signatures and classification trees: new tools for investigating the foraging ecology of seals. Can J Fish Aquat Sci 54:1377–1386

    Article  Google Scholar 

  • Summers LKM, Barnes SC, Fielding BA, Beysen C, Ilic V, Humphreys SM, Frayn KN (2000) Uptake of individual fatty acids into adipose tissue in relation to their presence in the diet. Am J Clin Nutr 71:1470–1477

    Google Scholar 

  • Terano T, Hirai A, Hamazaki T, Kobayashi S, Fujita T, Tamura Y, Kumagai A (1983) Effect of oral administration of highly purified eicosapentaenoic acid on platelet function, blood viscosity, and red cell deformability in healthy human subjects. Atherosclerosis 46:321–331

    Google Scholar 

  • Thomassen MS, Helgerud P, Norum KR (1985) Chain-shortening of erucic acid and microperoxisomal β-oxidation in rat small intestine. Biochem J 225:301–306

    Google Scholar 

  • Veerkamp JH, Zevenbergen JL (1986) Effect of dietary fat on total and peroxisomal fatty-acid oxidation in rat tissue. Biochim Biophys Acta 878:102–109

    Google Scholar 

  • Wang S, Koo SI (1993) Evidence for distinct metabolic utilization of stearic acid in comparison with palmitic and oleic acids in rats. J Nutr Biochem 4:594–601

    Article  Google Scholar 

  • Whyte M, Karmen A, Goodman DS (1963) Fatty acid esterification and chylomicron formation during fat absorption: 2 phospholipids. J Lipid Res 4:322–329

    Google Scholar 

  • Zilversmit DB (1965) The composition and structure of lymph chylomicrons in dog, rat, and man. J Clin Invest 44:1610–22

    Google Scholar 

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Acknowledgements

We thank J. Parsens and J. Eddington for help with the captive animal maintenance and blood sampling and W. Blanchard for assistance with statistical modelling. We thank W.D. Bowen for assistance with the initial planning of the study. We thank W.D. Bowen, S.M. Budge, H.W. Cook, G. Herzberg, S.L.C. Lang, and the three anonymous reviewers for very helpful comments on an earlier version of the manuscript. This study was supported by a Natural Sciences and Engineering Research Council (NSERC), Canada, Strategic Grant (No. STRO133825) and NSERC Research and Equipment Grants to S.J.I. This experiment was approved by the Dalhousie University Committee on Laboratory Animals.

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Correspondence to Margaret H. Cooper.

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Cooper, M.H., Iverson, S.J. & Heras, H. Dynamics of blood chylomicron fatty acids in a marine carnivore: implications for lipid metabolism and quantitative estimation of predator diets. J Comp Physiol B 175, 133–145 (2005). https://doi.org/10.1007/s00360-004-0469-6

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