Meyer Ottesen, C. A. et al. Early life history of the daubed shanny (Teleostei: Leptoclinus maculatus) in Svalbard waters. Mar. Biodivers. 41(3), 383–394 (2011).
Google Scholar
Murzina, S.A. Role of Lipids and Their Fatty Acid Components in Ecological and Biochemical Adaptations of Fish of the Northern Seas. Dr. Sci. Thesis (IPEE RAS, 2019).
Murzina, S. A. et al. Tiny but fatty: Lipids and fatty acids in the Daubed Shanny (Leptoclinus maculatus), a small fish in Svalbard waters. Biomolecules 10, 368 (2020).
Google Scholar
Falk-Petersen, S., Falk-Petersen, I. B. & Sargent, J. R. Structure and function of an unusal lipid storage organ in the Arctic fish Lumpenus maculatus Fries. Sarsia 71(1), 1–6 (1986).
Google Scholar
Murzina S.A. The Role of Lipids and Their Fatty Acid Components in the Biochemical Adaptations of the Daubed Shanny Leptoclinus maculatus F. of the Northwestern Coast of Svalbard. PhD Thesis 184 (IB KarRC RAS, 2010)
Pekkoeva, S. N. et al. Ecological role of lipids and fatty acids in the early postembryonic development of daubed shanny, Leptoclinus maculatus (Fries, 1838) from Kongsfjorden, West Spitsbergen in winter. Rus. J. Ecol. 48(3), 240–244 (2017).
Google Scholar
Hovde, S. C., Albert, O. T. & Nilssen, E. M. Spatial, seasonal and ontogenetic variation in diet of Northeast Arctic Greenland halibut (Reinhardtius hippoglossoides). ICES J. Mar. Sci. 59, 421–437 (2002).
Google Scholar
Labansen, A. L., Lydersen, C., Haug, T. & Kovacs, K. M. Spring diet of ringed seals (Phoca hispida) from northwestern Spitsbergen. Norway. ICES J. Mar. Sci. 64, 1246–1256 (2007).
Google Scholar
Moser, H. G. Morphological and functional aspect of marine fish larvae. in Marine Fish Larvae—Morphology, Ecology, and Relation to Fisheries (ed. Lasker, R.). 89–131. (University of Washington Press, 1981).
Moser, H. G. et al. Ontogeny and systematics of fishes. in American Society Ichthyologists Herpetologists Special Publication. Vol. 760 (Allen Press, 1984).
Webb, J. F. Larvae in fish development and evolution in The Origin and Evolution of Larval Forms. 109–158 (Academic Press, 1999).
Govoni, J. J., Olney, J. E., Markle, D. F. & Curtsinger, W. R. Observations on structure and evaluation of possible functions of the vexillum in larval Carapidae (Ophidiiformes). Bull. Mar. Sci. 34, 60–70 (1984).
Pekkoeva, S. N. et al. Fatty acid composition of the postlarval daubed shanny (Leptoclinus maculatus) during the polar night. Polar Biol. 43, 657–664 (2020).
Google Scholar
Pekkoeva, S. N. et al. Ecological groups of the Daubed Shanny Leptoclinus maculatus (Fries, 1838), an Arcto-boreal species, regarding growth and early development. Rus. J. Ecol. 49(3), 253–259 (2018).
Google Scholar
Schindelin, J. et al. Fiji: An open-source platform for biological-image analysis. Nat. Methods 9(7), 676–682 (2012).
Google Scholar
R Core Team. R: A Language and Environment for Statistical Computing. R Foundation for Statistical Computing. Version 12/2021. (R Foundation for Statistical Computing, 2020.)
Kabakoff, R. R in Action: Data Analysis and Graphics with R 588 (DMK Press, 2014).
Murzina, S. A. et al. Oogenesis and lipids in gonad and liver of daubed shanny (Leptoclinus maculatus) females from Svalbard waters. Fish Physiol. Biochem. 38(5), 1393–1407 (2012).
Google Scholar
Kondakova, E. A., Efremov, V. I. & Nazarov, V. A. Structure of the yolk syncytial layer in Teleostei and analogous structures in animals of the meroblastic type of development. Biol. Bull. 43(3), 208–215 (2016).
Google Scholar
Webster, M., Witkin, K. L. & Cohen-Fix, O. Sizing up the nucleus: Nuclear shape, size and nuclear-envelope assembly. J. Cell Sci. 122(10), 1477–1486 (2009).
Google Scholar
Jevtić, P., Edens, L. J., Vuković, L. D. & Levy, D. L. Sizing and shaping the nucleus: mechanisms and significance. Curr. Opin. Cell Biol. 28, 16–27 (2014).
Google Scholar
Kondakova, E. A., Efremov, V. I. & Kozin, V. V. Common and specific features of organization of the yolk syncytial layer of teleostei as exemplified in Gasterosteus aculeatus L. Biol. Bull. 46(1), 26–32 (2019).
Google Scholar
Enders, A. C. Reasons for diversity of placental structure. Placenta 30, 15–18 (2009).
Google Scholar
Carvalho, L. & Heisenberg, C. P. The yolk syncytial layer in early zebrafish development. Trends Cell Biol. 20(10), 586–592 (2010).
Google Scholar
Jaroszewska, M. & Dabrowski, K. Utilization of yolk: transition from endogenous to exogenous nutrition in fish. in Larval Fish Nutrition. 183–218 (2011).
Kondakova, E. A., Efremov, V. I. & Bogdanova, V. A. Structure of the yolk syncytial layer in the larvae of whitefishes: A histological study. Russ. J. Dev. Biol. 48(3), 176–184 (2017).
Google Scholar
Kondakova, E. A. & Bogdanova, V. A. The fate of the yolk syncytial layer during postembryonic development of Stenodus leucichthys nelma. Ann. Zool. Fenn. 58(4–6), 155–160 (2021).
Chanet, B. & Meunier, F. J. The anatomy of the thyroid gland among “fishes”: phylogenetic implications for the Vertebrata. Cybium 38(2), 89–116 (2014).
Zenzerov, V.S. Features of the Structure and Functioning of the Thyroid Gland of Fish in the Barents Sea. Doctor of Science Thesis. Vol. 42 (PetrGU, 2007).
Chalde, T. & Miranda, L. A. Pituitary–thyroid axis development during the larval–juvenile transition in the pejerrey Odontesthes bonariensis. J. Fish Biol. 91(3), 818–834 (2017).
Google Scholar
Otero, A. P., Rodrigues, R. V., Sampaio, L. A., Romano, L. A. & Tesser, M. B. Thyroid gland development in Rachycentron canadum during early life stages. An. Acad. Bras. Ciênc. 86(3), 1507–1516 (2014).
Google Scholar
Nilsson, M. & Fagman, H. Development of the thyroid gland. Development 144(12), 2123–2140 (2017).
Google Scholar
Eales, J. G. & Brown, S. B. Measurement and regulation of thyroidal status in teleost fish. Rev. Fish Biol. Fish. 3(4), 299–347 (1993).
Google Scholar
Raine, J. C. & Leatherland, J. F. Morphological and functional development of the thyroid tissue in rainbow trout (Oncorhynchus mykiss) embryos. Cell Tissue Res. 301(2), 235–244 (2000).
Google Scholar
de Jesus, E. G., Inui, Y. & Hirano, T. Cortisol enhances the stimulating action of thyroid hormones on dorsal fin-ray resorption of flounder larvae in vitro. Gen. Comp. Endocrinol. 79(2), 167–173 (1990).
Google Scholar
Inui, Y. & Miwa, S. Metamorphosis of flatfish (Pleuronectiformes). in Metamorphosis in Fish. 107–153 (Taylor & Francis, 2012)
Nemova, N. N., Rendakov, N. L., Pekkoeva, S. N., Nikerova, K. M. & Murzina, S. A. Dynamics of estradiol level during metamorphosis in the Daubed Shanny (Leptoclinus maculatus, Fries, 1838) from Spitsbergen Island. Dokl. Biol. Sci. 482, 188–190 (2018).
Google Scholar
Icardo, J. M. The teleost heart: A morphological approach in Ontogeny and Phylogeny of the Vertebrate Heart. 35–53 (Springer, 2012).
Icardo, J. M. Heart morphology and anatomy. in Fish Physiology. 1–54 (Academic Press, 2017).
Hu, N., Yost, H. J. & Clark, E. B. Cardiac morphology and blood pressure in the adult zebrafish. Anatomic. Rec. 264(1), 1–12 (2001).
Google Scholar
Icardo, J. M., Colvee, E., Cerra, M. C. & Tota, B. The bulbus arteriosus of stenothermal and temperate teleosts: A morphological approach. J. Fish Biol. 57, 121–135 (2000).
Google Scholar
Benjamin, M., Norman, D., Santer, R. M. & Scarborough, D. Histological, histochemical and ultrastructural studies on the bulbus arteriosus of the sticklebacks, Gasterosteus aculeatus and Pungitius pungitius (Pisces: Teleostei). J. Zool. 200(3), 325–346 (1983).
Google Scholar
Braun, M. H., Brill, R. W., Gosline, J. M. & Jones, D. R. Form and function of the bulbus arteriosus in yellowfin tuna (Thunnus albacares), bigeye tuna (Thunnus obesus) and blue marlin (Makaira nigricans): static properties. J. Exp. Biol. 206(19), 3311–3326 (2003).
Google Scholar
Icardo, J. M. Conus arteriosus of the teleost heart: Dismissed, but not missed. Anat. Rec. Part A Discov. Mol. Cell. Evolut. Biol. 288(8), 900–908 (2006).
Google Scholar
Tota, B. Vascular and metabolic zonation in the ventricular myocardium of mammals and fishes. Comp. Biochem. Physiol. A Physiol. 76(3), 423–437 (1983).
Google Scholar
Gardinal, M. V. B. et al. Myocardium arrangement and coronary vessel distribution in the ventricle of three neotropical freshwater teleosts. Zool. Sci. 35(4), 360–367 (2018).
Google Scholar
BuzeteGardinal, M. V. et al. Heart structure in the Amazonian teleost Arapaima gigas (Osteoglossiformes, Arapaimidae). J. Anat. 234(3), 327–337 (2019).
Google Scholar
Icardo, J. M. & Colvee, E. The atrioventricular region of the teleost heart. A distinct heart segment. Anatomic. Rec. Adv. Integr. Anat. Evolut. Biol. 294(2), 236–242 (2011).
Google Scholar
Kock, K. H. Antarctic icefishes (Channichthyidae): A unique family of fishes. A review, Part I. Polar Biol. 28, 862–895 (2005).
Google Scholar
Cocca, E. et al. Genomic remnants of alpha-globin genes in the hemoglobinless antarctic icefishes. Proc. Natl. Acad. Sci. 92(6), 1817–1821 (1995).
Google Scholar
di Prisco, G., Cocca, E., Parker, S. K. & Detrich, H. W. III. Tracking the evolutionary loss of hemoglobin expression by the white-blooded Antarctic icefishes. Gene 295(2), 185–191 (2002).
Google Scholar
Sidell, B. D. & O’Brien, K. M. When bad things happen to good fish: The loss of hemoglobin and myoglobin expression in Antarctic icefishes. J. Exp. Biol. 209(10), 1791–1802 (2006).
Google Scholar
Kaufman, Z. S. Adaptation of aquatic organisms to existence in high latitudes. Proc. Karelian Sci. Center Russ. Acad. Sci. 1, 3–19 (2015).
Jakubowski, M. Dimensions of respiratory surfaces of the gills and skin in the Antarctic white-blooded fish, Chaenocephalus aceratus Lönnberg (Chaenichthyidae). Z. Mikrosk.-Anat. Forschung. 96(1), 145–156 (1982).
Google Scholar
Graham, J. B. Air-breathing fishes: The biology, diversity, and natural history of air-breathing fishes. in Encyclopedia of Fish Physiology. 1861–1874 (Elsevier, 2011).
Maniatis, G. M. & Ingram, V. M. Erythropoiesis during amphibian metamorphosis: I. Site of maturation of erythrocytes in Rana catesbeiana. J. Cell Biol. 49(2), 372–379 (1971).
Google Scholar
Maruyama, K., Yasumasu, S. & Iuchi, I. Characterization and expression of embryonic and adult globins of the teleost Oryzias latipes (medaka). J. Biochem. 132(4), 581–589 (2002).
Google Scholar
Brownlie, A. et al. Characterization of embryonic globin genes of the zebrafish. Dev. Biol. 255(1), 48–61 (2003).
Google Scholar
Feng, J. et al. Channel catfish hemoglobin genes: Identification, phylogenetic and syntenic analysis, and specific induction in response to heat stress. Comp. Biochem. Physiol. D Genom. Proteom. 9, 11–22 (2014).
Google Scholar
Miwa, S. & Inui, Y. Thyroid hormone stimulates the shift of erythrocyte populations during metamorphosis of the flounder. J. Exp. Zool. 259(2), 222–228 (1991).
Google Scholar
Hansen, A., Reutter, K. & Zeiske, E. Taste bud development in the zebrafish, Danio rerio. Dev. Dyn. 223(4), 483–496 (2002).
Google Scholar
Wang, C. A. et al. The development of pharyngeal taste buds in Hucho taimen (Pallas, 1773) larvae. Iran. J. Fish. Sci. 15(1), 426–435 (2016).
Google Scholar
Fraser, G. J., Graham, A. & Smith, M. M. Conserved deployment of genes during odontogenesis across osteichthyans. Proc. R. Soc. Lond. Ser. B Biol. Sci. 271(1555), 2311–2317 (2004).
Google Scholar
Zambonino-Infante, J. L. et al. Ontogeny and physiology of the digestive system of marine fish larvae. in Feeding and Digestive Functions of Fishes. 281–348 (Science Publishers, 2008)
Rønnestad, I. et al. Feeding behaviour and digestive physiology in larval fish: Current knowledge, and gaps and bottlenecks in research. Rev. Aquac. 5, S59–S98 (2013).
Google Scholar
Wallace, R. A. & Selman, K. Physiological aspects of oogenesis in two species of stickelebacks, Gasterosteus aculeatus (L.) and Apeltes quadracus (Mitchill). J. Fish Biol. 14, 551–564 (1979).
Google Scholar
Source: Ecology - nature.com
