1. Bergé J-P, Barnathan G. Fatty Acids from Lipids of Marine Organisms: Molecular Biodiversity, Roles as Biomarkers, Biologically Active Compounds, and Economical Aspects. Adv Biochem Eng Biotechnol. 2005;96:49–125.
2. Parzanini C, Parrish C, Hamel J, Mercier A. Functional diversity and nutritional content in a deep-sea faunal assemblage through total lipid , lipid class , and fatty acid analyses. PLoS One. 2018;13(11):e0207395.
3. Parrish CC. Lipids in Marine Ecosystems. ISRN Oceanogr. 2013;2013:1–16.
4. Parrish CC, Abrajano T, Budge S, Helleur R, Hudson E, Pulchan K, et al. Lipid and Phenolic Biomarkers in Marine Ecosystems: Analysis and Applications. In: Wangersky P.J., editor. Marine Chemistry The Handbook of Environmental Chemistry (Vol 5 Series: Water Pollution). Springer Berlin Heidelberg; 2000.
5. Laender F De, Oevelen D Van, Frantzen S, Middelburg JJ, Soetaert K. Seasonal PCB bioaccumulation in an arctic marine ecosystem: a model analysis incorporating lipid dynamics, food-web productivity and migration. Environ Sci Technol. 2010 Jan;44(1):356–61.
6. Bianchi T, Canuel E. Chemical Biomarkers in Aquatic Ecosystems [Internet]. Princeton University Press; 2011.
7. Signa G, Di Leonardo R, Vaccaro A, Tramati CD, Mazzola A, Vizzini S. Lipid and fatty acid biomarkers as proxies for environmental contamination in caged mussels Mytilus galloprovincialis. Ecol Indic. 2015;57:384–94.
8. Brett M, Mueller-Navarra D, Persson J. Crustacean Zooplankton Fatty Acid Composition. In: Kainz M, Brett M, Arts M, editors. Lipids in Aquatic Ecosystems. New York: Springer; 2009. p. 115–46.
9. Martin-Creuzburg D, Elert E. Ecological Significance of Sterols in Aquatic Food Webs. In: Kainz M, Brett M, Arts M, editors. Lipids in Aquatic Ecosystems. New York: Springer; 2009. p. 43–64.
10. Parrish C. Essential fatty acids in aquatic food webs. In: Kainz M, Brett M, Arts M, editors. Lipids in aquatic ecosystems. New York: Springer; 2009. p. 309–26.
11. Maier SR, Bannister RJ, van Oevelen D, Kutti T. Seasonal controls on the diet, metabolic activity, tissue reserves and growth of the cold-water coral Lophelia pertusa. Coral Reefs 2020;39(1):173–87.
12. Phleger CF. Buoyancy in Marine Fishes: Direct and Indirect Role of Lipids. Am Zool. 1998;38(2):321–30.
13. Pond DW, Tarling GA. Phase transitions of wax esters adjust buoyancy in diapausing Calanoides acutus. Limnol Oceanogr. 2011;56(4):1310–8.
14. Giese AC. Lipids in the economy of marine invertebrates. Physiol Rev. 1966;46(2):244–98.
15. Joseph JD. Distribution and Composition of Lipids in Marine Invertebrates. In: Ackman RG, editor. Marine Biogenic Lipids, Fats and Oils. CRC Press, Boca Raton; 1989. p. 49–143.
16. Lee RF. Lipoproteins from the Hemolymph and Ovaries of Marine Invertebrates. In: Houlihan DF, Livingstone DR, Lee RF, editors. Advances in Comparative and Environmental Physiology. Berlin, Heidelberg: Springer Berlin Heidelberg; 1991. p. 187–207.
17. Kattner G, Hagen W. Lipid metabolism of the Antarctic euphausiid Euphausia crystallorophias and its ecological implications. Mar Ecol Prog Ser. 1998;170:203–13.
18. Heras H, Pollero RJ, Gonzalez-Baró MR, Pollero RJ. Lipid and fatty acid composition and energy partitioning during embryo development in the shrimp Macrobrachium borellii. Lipids 2000;35(6):645–51.
19. Viladrich N, Bramanti L, Tsounis G, Chocarro B, Martínez-Quitana A, Ambroso S, et al. Variation in lipid and free fatty acid content during spawning in two temperate octocorals with different reproductive strategies: surface versus internal brooder. Coral Reefs. 2016;35(3):1033–45.
20. Hansen M, Flatt T, Aguilaniu H. Reproduction, fat metabolism, and lifespan- What is the connection? Cell Metab. 2013;17(1):10–9.
21. Strathmann RR. Egg Size, Larval Development, and Juvenile Size in Benthic Marine Invertebrates. Am Nat. 1977;111(978):373–6.
22. Pechenik J. Delayed metamorphosis by larvae of benthic marine-invertebrates—does it occur? Is There a Price to Pay? Ophelia. 1990;32:63–94.
23. Harms J. Larval development and delayed metamorphosis in the hermit crab Clibanarius erythropus (Latreille) (Crustacea, Diogenidae). J Exp Mar Bio Ecol. 1992;156(2):151–60.
24. Harii S, Kayanne H, Takigawa HT, Hayashibara TH, Yamamoto M. Larval survivorship, competency periods and settlement of two brooding corals, Heliopora coerulea and Pocillopora damicornis. Mar Biol. 2002;141:39–46.
25. Doughty P, Shine R. Detecting life history trade-offs: measuring energy stores in “capital” breeders reveals costs of reproduction. Oecologia 1997;110(4):508–13.
26. Coma R, Ribes M, Gili J-M, Zabala M. An energetic approach to the study of life-history traits of two modular colonial benthic invertebrates. Mar Ecol Prog Ser. 1998;162:89–103.
27. Rossi S, Gili J-M, Coma R, Linares C, Gori A, Vert N. Temporal variation in protein, carbohydrate, and lipid concentrations in Paramuricea clavata (Anthozoa, Octocorallia): evidence for summer–autumn feeding constraints. Mar Biol. 2006;149(3):643–51.
28. Lee RF, Hagen W, Kattner G. Lipid storage in marine zooplankton. Mar Ecol Prog Ser. 2006;307:273–306.
29. Kattner G, Graeve M, Hagen W. Marine Biology. Mar Biol. 1994;644:18119.
30. Mourente G, Medina A, González S, Rodríguez A. Variations in lipid content and nutritional status during larval development of the marine shrimp Penaeus kerathurus. Aquaculture. 1995;130(2–3):187–99.
31. Marshall CT, Yaragina NA, Lambert Y, Kjesbu OS. Total lipid energy as a proxy for total egg production by fish stocks. Nature. 1999;402(6759):288–90.
32. Marshall CT, Yaragina NA, Ådlandsvik B, Dolgov A V. Reconstructing the stock-recruit relationship for Northeast Arctic cod using a bioenergetic index of reproductive potential. Can J Fish Aquat Sci. 2000;57(12):2433–42.
33. Dalsgaard J, St. John M, Kattner G, Müller-Navarra D, Hagen WBT-A in MB. Fatty acid trophic markers in the pelagic marine environment. In Academic Press; 2003. p. 225–340.
34. Bergquist PR, Lawson MP, Lavis A, Cambie RC. Fatty acid composition and the classification of the Porifera. Biochem Syst Ecol. 1984;12(1):63–84.
35. Djerassi C, Lam WK. Sponge Phospholipids. Acc Chem Res. 1991;24(3):69–75.
36. Thiel V, Blumenberg M, Hefter J, Pape T, Pomponi S, Reed J, et al. A chemical view of the most ancient metazoa - Biomarker chemotaxonomy of hexactinellid sponges. Naturwissenschaften. 2002;89(2):60–6.
37. Velosaotsy N, Genin E, Nongobienma R, Al-Lihaibi S, Kornprobst J-M, Vacelet J, et al. Phospholipid distribution and phospholipid fatty acids in four saudi red sea sponges. Boll Mus Ist Biol Univ Genova. 2004;68:639–45.
38. Rod’kina SA. Fatty acids and other lipids of marine sponges. Russ J Mar Biol. 2005;31(Suppl. 1):S49–60.
39. Blumenberg M, Michaelis W. High occurrences of brominated lipid fatty acids in boreal sponges of the order Halichondrida. Mar Biol. 2007;150(6):1153–60.
40. Genin E, Wielgosz-Collin G, Njinkoué JM, Velosaotsy NE, Kornprobst JM, Gouygou JP, et al. New trends in phospholipid class composition of marine sponges. Comp Biochem Physiol - B Biochem Mol Biol. 2008;150(4):427–31.
41. Müller W, Rottmann M, Diehl-Seifert B, Kurelec B, Uhlenbruck G, Schröder HC. Role of the aggregation factor in the regulation of phosphoinositide metabolism in sponges. Possible consequences on calcium efflux and on mitogenesis. J Biol Chem. 1987;262(20):9850–8.
42. Weissmann G, Riesen W, Davidson S, Waite M. Stimulus-response coupling in marine sponge cell aggregation: lipid metabolism and the function of exogenously added arachidonic and docosahexaenoic acids. Biochim Biophys Acta. 1988;960(3):351–64.
43. Zivanovic A, Pastro NJ, Fromont J, Thomson M, Skropeta D. Kinase inhibitory, haemolytic and cytotoxic activity of three deep-water sponges from North Western Australia and their fatty acid composition. Nat Prod Commun. 2011;6(12):1921–4.
44. Shaaban M, Abd-Alla HI, Hassan AZ, Aly HF, Ghani MA. Chemical characterization, antioxidant and inhibitory effects of some marine sponges against carbohydrate metabolizing enzymes. Org Med Chem Lett. 2012;2(1):30.
45. Botić T, Cör D, Anesi A, Guella G, Sepčić K, Janussen D, et al. Fatty acid composition and antioxidant activity of Antarctic marine sponges of the genus Latrunculia. Polar Biol. 2015;38(10):1605–12.
46. Bennett H, Bell JJ, Davy SK, Webster NS, Francis DS. Elucidating the sponge stress response; lipids and fatty acids can facilitate survival under future climate scenarios. Glob Chang Biol. 2018;24(7):3130–44.
47. Carballeira NM. New advances in fatty acids as antimalarial, antimycobacterial and antifungal agents. Prog Lipid Res. 2008;47(1):50–61.
48. Kikuchi H, Tsukitani Y, Manda T, Fujii T, Nakanishi H, Kobayashi M, et al. Marine natural Products. X. Pharmacologically active glycolipids from the Okinawan marine sponge Phyllospongia foliascens (Pallas). Chem Pharm Bull. 1982;30:3544–7.
49. Natori T, Morita M, Akimoto K, Koezuka Y. Agelasphins, novel antitumor and immunostimulatory cerebrosides from the marine sponge Agelas mauritianus. Tetrahedron. 1994;50(9):2771–84.
50. Costantino V, Fattorusso E, Mangoni A, Di Rosa M, Ianaro A. Glycolipids from Sponges. 6. Plakoside A and B, two unique prenylated glycosphingolipids with Immunosuppressive activity from the marine sponge Plakortis simplex. J Am Chem Soc. 1997;119(51):12465–70.
51. Costantino V, Fattorusso E, Imperatore C, Mangoni A. Glycolipids from sponges. 11. Isocrasserides, novel glycolipids with a five-membered cyclitol widely distributed in marine sponges. J Nat Prod. 2002;65(6):883–6.
52. Maldonado M, Riesgo A. Reproduction in Porifera: a synoptic overview. Treballs la Soc Catalana Biol. 2008;59:29–49.
53. Sciscioli M, Lepore E, Scalera-Liaci L, Gherardi M. Indagine ultrastrutturale sugli ovociti di Erylus discophorus (Schmidt) (Porifera, Tetractinellida). Oebalia. 1989;15:939–941.
54. Sciscioli M, Liaci LS, Lepore E, Gherardi M, Simpson TL. Ultrastructural study of the mature egg of the marine sponge Stelletta grubii (porifera demospongiae). Mol Reprod Dev. 1991 Apr 1;28(4):346–50.
55. Riesgo A, Taboada S, Sánchez-Vila L, Solà J, Bertran A, Avila C. Some like it fat: comparative ultrastructure of the embryo in two demosponges of the genus Mycale (order Poecilosclerida) from Antarctica and the Caribbean. PLoS One 2015;10(3):e0118805.
56. Watanabe Y. The Development of Two Species of Tetilla (Demosponge). NSR O U. 1978;29(1):71–106.
57. Gaino E, Sarà M. An ultrastructural comparative study of the eggs of two species of Tethya (Porifera, Demospongiae). Invertebr Reprod Dev. 1994;26(2):99–106.
58. Maldonado M, Riesgo A. Gametogenesis, embryogenesis, and larval features of the oviparous sponge Petrosia ficiformis (Haplosclerida, Demospongiae). Mar Biol. 2009;156(10):2181–97.
59. Lanna E, Klautau M. Oogenesis and spermatogenesis in Paraleucilla magna (Porifera, Calcarea). Zoomorphology. 2010;129(4):249–61.
60. Koutsouveli V, Taboada S, Moles J, Cristobo J, Ríos P, Bertran A, et al. Insights into the reproduction of some Antarctic dendroceratid, poecilosclerid, and haplosclerid demosponges. PLoS One. 2018;13(2):1–24.
61. Fell PE. The involvement of nurse cells in oogenesis and embryonic development in the marine sponge, Haliclona ecbasis. J Morphol. 1969;127(2):133–49.
62. Simpson T. The cell biology of sponges. Springer, New York. 1984;
63. Bellairs R. The structure of the yolk of the hen’s egg as studied by electron microscopy : i. the yolk of the unincubated egg. J Biophys Biochem Cytol. 1961;11(1):207–25.
64. Maldonado M, Riesgo A. Reproduction in the phylum Porifera: a synoptic overview. Treballs la SCB. 2008;59:29–49.
65. Ereskovsky A. The comparative embryology of sponges. Springer; 2010. 1–323 p.
66. Watanabe Y. The Development of Two Species of Tetilla (Demosponge). Nat Sci Rep. 1978;29:71–106.
67. Sarà A, Cerrano C, Sarà M. Viviparous development in the Antarctic sponge Stylocordyla borealis Loven, 1868. Polar Biol. 2002;25(6):425–31.
68. Busch K, Wurz E, Rapp HT, Bayer K, Franke A, Hentschel U. Chloroflexi Dominate the Deep-Sea Golf Ball Sponges Craniella zetlandica and Craniella infrequens Throughout Different Life Stages. Front Mar Sci. 2020;7:674.
69. Koopmans M, van Rijswijk P, Boschker HTS, Marco H, Martens D, Wijffels RH. Seasonal Variation of Fatty Acids and Stable Carbon Isotopes in Sponges as Indicators for Nutrition: Biomarkers in Sponges Identified. Mar Biotechnol. 2015;17(1):43–54.
70. Lüskow F, Kløve-Mogensen K, Tophøj J, Pedersen LH, Riisgård HU, Eriksen NT. Seasonality in lipid content of the demosponges Halichondria panicea and H. bowerbanki at two study sites in temperate Danish waters. Front Mar Sci. 2019; (6):1–7.
71. Reiswig H. Population dynamics of three jamaican demospongiae. Bull Mar Sci. 1973;23:191–226.
72. Elvin DW. Seasonal Growth and Reproduction of an Intertidal Sponge, Haliclona permollis (Bowerbank). Univ Chicago Press. 1976;151(1):108–25.
73. Elvin DW. The relationship of seasonal changes in the biochemical components to the reproductive behavior of the intertidal sponge, Haliclona permollis. biol Bull. 1979;156:47–61.
74. Schmidt O. Die Spongien der Küste von Algier. Mit Nachträgen zu den Spongien des Adriatischen Meeres (Drittes Supplement). (Wilhelm Engelmann: Leipzig): i-iv, 1-44, pls I-V. 1868;
75. Ivanisevic J, Pérez T, Ereskovsky A V, Barnathan G, Thomas OP. Lysophospholipids in the Mediterranean Sponge Oscarella tuberculata: Seasonal Variability and Putative Biological Role. J Chem Ecol. 2011;37(5):537.
76. Klitgaard AB. The fauna associated with outer shelf and upper slope sponges (Porifera, demospongiae) at the Faroe islands, North-eastern Atlantic. 1995;80(1):1-22.
77. Klitgaard AB, Tendal O. Distribution and species composition of mass occurrences of large-sized sponges in the northeast Atlantic. Prog Oceanogr. 2004;61:57–98.
78. Kutti T, Bannister RJ, Fosså JH. Community structure and ecological function of deep-water sponge grounds in the Traenadypet MPA — Northern Norwegian continental shelf. 2013;69:21–30.
79. Pile A, Young C. The natural diet of a hexactinellid sponge: Benthic–pelagic coupling in a deep-sea microbial food web. Deep Sea Res Part I Oceanogr Res Pap. 2006;53:1148–56.
80. Yahel G, Whitney F, Reiswig HM, Eerkes-Medrano DI, Leys SP. In situ feeding and metabolism of glass sponges (Hexactinellida, Porifera) studied in a deep temperate fjord with a remotely operated submersible. Limnol Oceanogr. 2007;52(1):428–40.
81. Hoffmann F, Radax R, Woebken D, Holtappels M, Lavik G, Rapp HT, et al. Complex nitrogen cycling in the sponge Geodia barretti. Environ Microbiol. 2009;11(9):2228–43.
82. Cathalot C, Van Oevelen D, Cox TJS, Kutti T, Lavaleye M, Duineveld G, et al. Cold-water coral reefs and adjacent sponge grounds: hotspots of benthic respiration and organic carbon cycling in the deep sea. Front Mar Sci. 2015;2:1–12.
83. Kahn A, Yahel G, Chu J, Tunnicliffe V, Leys S. Benthic grazing and carbon sequestration by deep-water glass sponge reefs. Limnol Oceanogr. 2015;60:78–88.
84. Rooks C, Fang JK-H, Mørkved PT, Zhao R, Rapp HT, Xavier JR, et al. Deep-sea sponge grounds as nutrient sinks: denitrification is common in boreo-Arctic sponges. Biogeosciences. 2020;17(5):1231–45.
85. Linnaeus C. Systema naturae per regna tria naturae: secundum classes, ordines, genera, species, cum characteribus, differentiis, synonymis, locis. Ed. 12. 1., Regnum Animale. 1 & 2. Holmiae, Laurentii Salvii. 1767. pp. 533-1327
86. Spetland F, Rapp HT, Hoffmann F, Tendal OS. Sexual reproduction of Geodia barretti Bowerbank, 1858 (Porifera, Astrophorida) in two Scandinavian fjords. In: Custódio M, Lôbo-Hajdu G, Hajdu E, Muricy G, editors. Porifera Research: Biodiversity, Innovation, Sustainability. Série Livros. Museu Nacional, Rio de Janeiro.; 2007. p. 613–20.
87. Koutsouveli V, Cárdenas P, Conejero M, Rapp HT, Riesgo A. Reproductive Biology of Geodia Species (Porifera, Tetractinellida) From Boreo-Arctic North-Atlantic Deep-Sea Sponge Grounds. Front Mar Sci. 2020;7:1–22.
88. Bowerbank JS. On the Anatomy and Physiology of the Spongiadae. Part I. On the Spicula. Philos Trans R Soc. 1858;
89. Wassmann P. Dynamics of primary production and sedimentation in shallow fjords and polls of western Norway. Oceanogr Mar Biol an Annu Rev. 1991;29:87–154.
90. Wassmann P, Svendsen H, Keck A, Reigstad M. Selected aspects of the physical oceanography and particle fluxes in fjords of northern Norway. J Mar Syst. 1996;8(1):53–71.
91. Bamstedt U. Life cycle, seasonal vertical distribution and feeding of Calanus finmarchicus in Skagerrak coastal water. Mar Biol. 2000;137(2):279–89.
92. Linnaeus C. Systema Naturae per regna tria naturae, secundum classes, ordines, genera, species, cum characteribus, differentiis, synonymis, locis. Vol. 1, Editio decima, reformata. Laurentius Salvius: Holmiae. 1758. 824 p.
93. Witte U. Seasonal reproduction in deep-sea sponges - triggered by vertical particle flux? Mar Biol. 1996;124(4):571–81.
94. Southwood TR. Habitat , the Templet for Ecological Strategies. J Anim Ecol. 1977;46(2):336–65.
95. Clarke A. A reappraisal of the concept of metabolic cold adaptation in polar marine invertebrates. Biol J Linn Soc. 1980;14(1):77–92.
96. Eckelbarger KJ, Watling L. Role of Phylogenetic Constraints in Determining Reproductive Patterns in Deep-Sea Invertebrates. Invertebr Biol. 1995;114(3):256–69.
97. Busch K, Taboada S, Riesgo A, Koutsouveli V, Ríos P, Cristobo J, et al. Population connectivity of fan-shaped sponge holobionts in the deep Cantabrian Sea. Deep Sea Res Part I Oceanogr Res Pap. 2020;103427.
98. Riesgo A, Maldonado M. Ultrastructure of oogenesis of two oviparous demosponges: Axinella damicornis and Raspaciona aculeata (Porifera). Tissue Cell. 2009;41(1):51–65.
99. Whiteley NM, Taylor EW, el Haj AJ. A comparison of the metabolic cost of protein synthesis in stenothermal and eurythermal isopod crustaceans. Am J Physiol. 1996;271:R1295-303.
100. Pace DA, Manahan DT. Cost of protein synthesis and energy allocation during development of Antarctic sea urchin embryos and larvae. Biol Bull. 2007;212:115–29.
101. Sciscioli M, Lepore E, Gherardi M, Liaci LS. Transfer of symbiotic bacteria in the mature oocyte of Geodia cydonium (Porifera, Demosponsgiae): An ultrastructural study. Cah Biol Mar. 1994;35(4):471–8.
102. Bronson F. Mammalian reproductive biology. Chicago: University of Chicago Press; 1989.
103. McWilliams SR, Guglielmo C, Pierce B, Klaassen M. Flying, fasting, and feeding in birds during migration: a nutritional and physiological ecology perspective. J Avian Biol. 2004;35(5):377–93.
104. Derickson WK. Lipid Storage and Utilization in Reptiles. Am Zool. 1976;16(4):711–23.
105. Fraser AJ. Triacylglycerol Content as a Condition Index for Fish, Bivalve, and Crustacean Larvae. Can J Fish Aquat Sci. 1989;46(11):1868–73.
106. Bonnet X, Naulleau G, Mauget R. The influence of body condition on 17-beta estradiol levels in relation to vitellogenesis in female Vipera aspis (Reptilia, Viperidae). Gen Comp Endocrinol. 1994;93(3):424–37.
107. Duggan A, Paolucci M, Tercyak A, Gigliotti M, Small D, Callard I. Seasonal variation in plasma lipids, lipoproteins, apolipoprotein A-I and vitellogenin in the freshwater turtle, Chrysemys picta. Comp Biochem Physiol Part A, Mol & Integr Physiol. 2001;130(2):253–69.
108. Lance VA, Place AR, Grumbles JS, Rostal DC. Variation in plasma lipids during the reproductive cycle of male and female desert tortoises, Gopherus agassizii. J Exp Zool. 2002;293(7):703–11.
109. Kawazu I, Kino M, Yanagisawa M, Maeda K, Nakada K, Yamaguchi Y, et al. Signals of Vitellogenesis and Estrus in Female Hawksbill Turtles. Zoolog Sci. 2015;32(1):114–8.
110. Teshima S ichi, Kanazawa A. Variation in Lipid Compositions during the Ovarian Maturation of the Prawn. Nippon Suisan Gakkaishi. 1983;49(6):957–62.
111. Clarke A, Brown JH, Holmes LJ. The biochemical composition of eggs from Macrobrachium rosenbergii in relation to embryonic development. Comp Biochem Physiol Part B Comp Biochem. 1990;96(3):505–11.
112. Allen W. Amino Acid and Fatty Acid Composition of Tissues of the Dungeness Crab (Cancer magister). J Fish Res. 1971;28:1191–5.
113. Rosa R, Nunes ML. Tissue biochemical composition in relation to the reproductive cycle of deep-sea decapod Aristeus antennatus in the Portuguese south coast. J Mar Biol Assoc.2003;83(5):963–70.
114. Balgoma D, Pettersson C, Hedeland M. Common Fatty Markers in Diseases with Dysregulated Lipogenesis. Trends Endocrinol Metab. 2019;30(5):283–5.
115. Kent C. Eukaryotic phospholipid biosynthesis. Annu Rev Biochem. 1995;64(1):315–43.
116. Coleman RA, Lee DP. Enzymes of triacylglycerol synthesis and their regulation. Prog Lipid Res. 2004;43(2):134–76.
117. Bell RM, Coleman RA. Enzymes of glycerolipid synthesis in eukaryotes. Annu Rev Biochem. 1980;49:459–87.
118. Mathews C, van Holde K, Appling D, Anthony-Cahill S. Biochemistry. 4th ed. Pearson; 2019. 1368 p.
119. Gavaud J. Histochemical identification of ovarian lipids during vitellogenesis in the lizard Lacerta vivipara . Can J Zool. 1991;69(5):1389–92.
120. Chapman MJ. Animal lipoproteins: Chemistry, structure, and comparative aspects. J Lipid Res. 1980;21(7):789–853.
121. Dolphin PJ, Ansari AQ, Lazier CB, Munday KA, Akhtar M. Studies on the induction and biosynthesis of vitellogenin, an oestrogen-induced glycolipophosphoprotein. Biochem J. 1971;124(4):751–8.
122. Riesgo A, Farrar N, Windsor PJ, Giribet G, Leys SP. The analysis of eight transcriptomes from all poriferan classes reveals surprising genetic complexity in sponges. Mol Biol Evol. 2014;31(5):1102–20.
123. Koutsouveli V, Cárdenas P, Santodomingo N, Marina A, Morato E, Rapp HT, et al. The molecular machinery of gametogenesis in Geodia demosponges (Porifera): evolutionary origins of a conserved toolkit across animals. Mol Biol Evol. 2020;
124. Wanders RJA. Peroxisomes, lipid metabolism, and peroxisomal disorders. Mol Genet Metab. 2004;83(1):16–27.
125. Wanders RJA, Waterham HR, Ferdinandusse S. Metabolic Interplay between Peroxisomes and Other Subcellular Organelles Including Mitochondria and the Endoplasmic Reticulum. Vol. 3, Frontiers in Cell and Developmental Biology . 2016. p. 83.
126. Talley J, Mohiuddin S. Biochemstry, Fatty Acid Oxidation. StatPearls. 2020.
127. Reiswig HM. Particle Feeding in Natural Populations of Three Marine Demosponges. Biol Bull. 1971;141(3):568–91.
128. Sugimoto Y, Inazumi T, Tsuchiya S. Roles of prostaglandin receptors in female reproduction. J Biochem. 2015 Feb 1;157(2):73–80.
129. Reynolds ES. The use of lead citrate at high PH as an electron-opaque stain in electron microscopy. J Cell Biol. 1963;17(1):208–12.
130. Schneider CA, Rasband WS, Eliceiri KW. NIH Image to ImageJ: 25 years of image analysis. Nat Methods. 2012 Jul;9(7):671–5.
131. Bligh, E.G. and Dyer WJ. Canadian Journal of Biochemistry and Physiology. Can J Biochem Physiol. 1959;37(8):911–7.
132. Balgoma D, Zelleroth S, Grönbladh A, Hallberg M, Pettersson C, Hedeland M. Anabolic androgenic steroids exert a selective remodeling of the plasma lipidome that mirrors the decrease of the de novo lipogenesis in the liver. Metabolomics. 2020;16(1):12.
133. Kolmert J, Piñeiro-Hermida S, Hamberg M, Gregory JA, López IP, Fauland A, et al. Prominent release of lipoxygenase generated mediators in a murine house dust mite-induced asthma model. Prostaglandins Other Lipid Mediat. 2018 Jul;137:20–9.
134. Balgoma D, Yang M, Sjödin M, Snowden S, Karimi R, Levänen B, et al. Linoleic acid-derived lipid mediators increase in a female-dominated subphenotype of COPD. Eur Respir J. 2016;47(6):1645 – 1656.
135. Smith CA, Want EJ, O’Maille G, Abagyan R, Siuzdak G. XCMS: processing mass spectrometry data for metabolite profiling using nonlinear peak alignment, matching, and identification. Anal Chem. 2006 Feb;78(3):779–87.
136. Tautenhahn R, Böttcher C, Neumann S. Highly sensitive feature detection for high resolution LC/MS. BMC Bioinformatics. 2008;9(1):504.
137. Fahy E, Sud M, Cotter D, Subramaniam S. LIPID MAPS online tools for lipid research. Nucleic Acids Res. 2007 Aug 1;35:W606-12.
138. Böcker S, Letzel MC, Lipták Z, Pervukhin A. SIRIUS: decomposing isotope patterns for metabolite identification. Bioinformatics. 2008 Nov 17;25(2):218–24.
139. Bolger AM, Lohse M, Usadel B. Trimmomatic: a flexible trimmer for Illumina sequence data. Bioinformatics [Internet]. 2014;30:2114–2120.
140. Grabherr MG, Haas BJ, Yassour M, Levin JZ, Thompson DA, Amit I, et al. Trinity: reconstructing a full-length transcriptome without a genome assembly from RNA-Seq data. Nat Biotechnol. 2011;29(7):644–52.
141. Simão FA, Waterhouse RM, Ioannidis P, Kriventseva E V, Zdobnov EM. BUSCO: assessing genome assembly and annotation completeness with single-copy orthologs. Bioinformatics. 2015;31(19):3210–2.
142. Langmead B, Salzberg SL. Fast gapped-read alignment with Bowtie 2. Vol. 9, Nature methods. 2012. p. 357–9.
143. Li B, Dewey CN. RSEM: accurate transcript quantification from RNA-Seq data with or without a reference genome. BMC Bioinformatics. 2011;12(1):323.
144. Robinson MD, McCarthy DJ, Smyth GK. edgeR: a Bioconductor package for differential expression analysis of digital gene expression data. Bioinformatics. 2009;26(1):139–40.
145. McCarthy DJ, Chen Y, Smyth GK. Differential expression analysis of multifactor RNA-Seq experiments with respect to biological variation. Nucleic Acids Res. 2012;40(10):4288–97.
146. Altschul SF, Madden TL, Schäffer AA, Zhang J, Zhang Z, Miller W, et al. Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. Nucleic Acids Res. 1997;25(17):3389–402.
147. Boeckmann B, Bairoch A, Apweiler R, Blatter M-C, Estreicher A, Gasteiger E, et al. The SWISS-PROT protein knowledgebase and its supplement TrEMBL in 2003. Nucleic Acids Res. 2003;31(1):365–70.
148. Buchfink B, Xie C, Huson DH. Fast and sensitive protein alignment using DIAMOND. Nat Methods. 2014 Nov 17;12:59.
149. Conesa A, Götz S, García-Gómez JM, Terol J, Talón M, Robles M. Blast2GO: A universal tool for annotation, visualization and analysis in functional genomics research. Bioinformatics. 2005;21(18):3674-3676.
150. Kanehisa M, Goto S. KEGG: kyoto encyclopedia of genes and genomes. Nucleic Acids Res. 2000;28(1):27–30.