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    المصدر: Scientia Marina; Vol. 73 No. 1 (2009); 173-182 ; Scientia Marina; Vol. 73 Núm. 1 (2009); 173-182 ; 1886-8134 ; 0214-8358 ; 10.3989/scimar.2009.73n1

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Response of muscle-based biochemical condition indices to short-term variations in food availability in post-flexion reared sea bass (Dicentrarchus labrax L.) larvae. J. Fish. Biol.; Dabrowski, K. and K. Tsukamoto. – 1986. Tetracycline tagging in coregonid embryos and larvae. J. Fish. Biol., 29: 691-698. doi:10.1111/j.1095-8649.1986.tb04985.x; Ferron, A. and W.C. Leggett. – 1994. An appraisal of condition measures for marine fish larvae. Adv. Mar. Biol., 30: 217-303. doi:10.1016/S0065-2881(08)60064-4; Folkvord, A., G. Blom, A. Johannssen and E. Moksness. – 2000. Growth-dependent age estimation in herring (Clupea harengus L.) larvae. Fish. Res., 46:91-103. doi:10.1016/S0165-7836(00)00136-3; Folkvord, A., A. Johannessen and E. Moksness. – 2004. Temperature dependent otolith growth in herring (Clupea harengus L.) larvae. Sarsia, 89: 297-310. doi:10.1080/00364820410002532; Geffen, A.J. – 1982. Otolith ring deposition in relation to growth rate in herring (Clupea harengus) and turbot (Scophthalmus maximus) larvae. Mar. Biol., 71: 317-326. doi:10.1007/BF00397048; Geffen, A. – 1992. Validation of otolith increment deposition rate. In: D.K.Stevenson and S.E. Campana (eds). Otolith microstructure examination and analysis. Can. Spec. Publ. Fish. Aquat. Sci., 117: 101-113.; Geffen, A.J. – 1995. Growth and otolith microstructure of cod (Gadus morhua L.) larvae. J. Plankton Res., 17: 783-800. doi:10.1093/plankt/17.4.783; González-Quirós, R., I. Munuera and A. Folkvord. – 2007. Cell cycle analysis of brain cells as a growth index in larval cod at different feeding conditions and temperatures. Sci. Mar., 71(3): 485-497.; Govoni, J.J., A.J. Chester, D.E. Hoss and P.B. Ortner. – 1985. An observation of episodic feeding and growth of larval Leiostomus xanthurus in the northern Gulf of Mexico. J. Plankton Res., 7: 137-146. doi:10.1093/plankt/7.1.137; Gutiérrez, E. and B. 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Age, growth rate, and growth trajectory determined from otolith microstructure of southern bluefin tuna, Thunnus maccoyii, larvae. Mar. Ecol. Prog. Ser., 63: 93-104. doi:10.3354/meps063093; Karakiri, M. – 1989. Daily growth patterns in otoliths of early stage plaice: preparation techniques and interpretation of readings. In: L. Schröeder (ed.), New trends in ichthyology. Paul Parey Verlag, Hamburg.; Karakiri, M. and H. von Westernhagen. – 1989. Daily growth patterns in otoliths of larval and juvenile plaice (Pleuronectes platessa L.): influence of temperature, salinity, and light conditions. Rapp. P-v. Réun. Cons. Int. Explor. Mer., 191: 376-382.; McVey, J.P. (ed.) – 1983. CRC Handbook of Mariculture. CRC Pr Llc, Boca Raton, Florida, USA.; Maillet, G.L. and D.M. Checkley. – 1990. Effects of starvation on the frequency of formation and width of growth increments in sagittae of laboratory-reared Atlantic menhaden Brevoortia tyrannus larvae. Fish. Bull. US, 88(1): 155-165.; Maillet, G.L. and D.M. Checkley. – 1991. Storm-related variation in the growth rate of otoliths of larval Atlantic menhaden Brevoortia tyrannus: time series analysis of biological and physical variables and implications for larval growth and mortality. Mar. Ecol. Prog. Ser., 79: 1-16. doi:10.3354/meps079001; Marangos, Ch., H. Yagi and H.J. Ceccaldi. – 1986. Rôle de la température et de la salinité sur le tax de survie et la morphogenèse au cours du développement embryonnaire chez les eufs du loup de mer, Dicentrarchus labrax (Linaeus, 1758) (Pisces, Teleostei, Serranidae). Aquaculture, 54: 287-300. doi:10.1016/0044-8486(86)90273-5; Methot, R.D. Jr. – 1981. Spatial covariation of daily growth of larval northern anchovy Engraulis mordax, and northern lampfish, Stenobrachius leucopsarus. Rapp. P-v. Réun. Cons. Int. Explor. Mer. 178: 424-431.; Methot, R.D. Jr. and D. Kramer. – 1979. Growth of northern anchovy, Engraulis mordax, larvae in the sea. Fish. Bull. US, 77: 413-423.; Molony, B.W. and J.H. Choat. – 1990. Otolith increment widths and somatic growth rate: the presence of a time lag. J. Fish Biol., 37(4): 541-551; Morales-Nin, B. – 1985. Daily growth increments in the otoliths of Dicentrarchus labrax. Rapp. Comm. Int. Mer. Medit., 29(8): 95-97.; Morales-Nin, B. – 1987. The influence of environmental factors on microstructure of otoliths of three demersal fish species off Namibia. S. Afr. J. Mar. Sci., 5: 255-262.; Morales-Nin, B. – 2000. Review of the growth regulation processes of otolith daily increment formation. Fish. Res., 46: 53-67. doi:10.1016/S0165-7836(00)00133-8; Neilson, J.D. and G.H. Geen. – 1985. Effects of feeding regimes and diel temperature cycles on otolith increment formation in juvenile chinook salmon, Oncorhynchus tshawytscha. Fish. Bull. US, 83: 91-101.; Olivar, M.P., P.P. Ambrosio and I.A. Catalán. – 2000. A closed water recirculation system for ecological studies in marine fish larvae: growth and survival of sea bass larvae fed with live prey. Aquat. Liv. Res. 13(1): 29-35. doi:10.1016/S0990-7440(00)00136-4; Otterlei, E., A. Folkvord and G. Nyhammer. – 2002. Temperature dependent otolith growth of larval and early juvenile atlantic cod (Gadus morhua). ICES J. Mar. Sci., 59(2): 401-410. doi:10.1006/jmsc.2001.1170; Pannella, G. – 1980. Growth patterns in fish sagittae. In: D.C. Rhoads and R.A. Lutz (eds.), Skeletal growth of aquatic organisms, pp. 519-560. Plenum Press, New York.; Planes, S., P. Laval and R. Lecomte-Finiger. – 1991. An otolithic image analysis method for ageing and estimating growth of larvae and juveniles of sea-bass (Dicentrarchus labrax (Linnaeus, 1758): preliminary results. Sci. Mar., 55(4): 591-597.; Powell, A.B., A.J. Chester, J.J. Govoni, S.M. Warlen. – 1990. Nutritional condition of spot larvae associated with the Mississippi River plume. Trans. Am. Fish. Soc., 119: 957-965. doi:10.1577/1548-8659(1990)1192.3.CO;2; Ré, P., H.C. Rosa and M.T. Dinis. – 1986. Daily microgrowth increments in the sagittae of Dicentrarchus labrax (L.) larvae under controlled conditions. Invest. Pesq., 50(3): 397-402.; Regner, S. and J. Dulcˇic´. – 1994. Growth of sea bass, Dicentrarchus labrax, larval and juvenile stages and their otoliths under quasisteady temperature conditions. Mar. Biol., 119: 169-177. doi:10.1007/BF00349553; Rice, J.A., L.B. Crowder and M.E. Holey. – 1987. Exploration of mechanisms regulating larval survival in Lake Michigan bloater: a recruitment analysis based on characteristics of individual larvae. Trans. Am. Fish. Soc., 116: 703-718. doi:10.1577/1548-8659(1987)1162.0.CO;2; Secor, D.H., M.G. White and J.M. Dean. – 1991. Immersion marking of larval and juvenile hatchery-produced striped bass with oxytetracycline. Trans. Am. Fish. Soc., 120: 261-266. doi:10.1577/1548-8659(1991)1202.3.CO;2; Suthers, I.M. – 1996. Spatial variability of recent otolith growth and RNA indices in pelagic juvenile Diaphus kapalae (Myctophidae): an effect of flow disturbance near an island? Mar. Freshwat. Res., 47: 273-282. doi:10.1071/MF9960273; Suthers, I.M. – 1998. Bigger? Fatter? Or is faster growth better? Considerations on condition in larval and juvenile coral-reef fish. Aust. J. Ecol., 23: 265-273. doi:10.1111/j.1442-9993.1998.tb00730.x; Suthers, I.M., K.T. Frank and S.C. Campana. – 1989. Spatial comparison of recent growth in post-larval cod (Gadus morhua) off southwestern Nova Scotia: inferior growth in a presumed nursery area. Can. J. Fish. Aquat. Sci., 46(Suppl. 1): 13-21.; Suthers, I.M. and S. Sundby. – 1993. Dispersal and growth of pelagic juvenile Arcto-Norwegian cod (Gadus morhua) inferred from otolith microstructure and water temperature. ICES J. Mar. Sci., 50: 261-270. doi:10.1006/jmsc.1993.1028; Swaddle, J.P. and M.S. Witter. – 1994. Food, feathers and fluctuating asymmetries. Proc. R. Soc. Lond. B, 255: 147-152. doi:10.1098/rspb.1994.0021; Taubert, B.D. and D.W. Coble. – 1977. Daily rings in otoliths of three species of Lepomis and Tilapia mossambica. J. Fish. Res. Board. Can., 34: 332-340.; Tsukamoto, K., H. Kuwada, J. Hirokawa, M. Oya, S. Sekiya, H. Fujimoto and K. Imaizumi. – 1989. Size-dependent mortality of red sea bream, Pagrus major, juveniles released with fluorescent otolith-tags in New Bay, Japan. J. Fish. Biol., 35 (Suppl. A): 59-69. doi:10.1111/j.1095-8649.1989.tb03393.x; Volk, E.C., R.C. Wissmar, C.A. Simestadand D.M. Eggers. – 1984. Relationship between otolith microstructure and the growth of juvenile chum salmon (Onchorhynchus keta) under different prey rations. Can. J. Fish. Aquat. Sci., 41: 126-133. doi:10.1139/f84-012; Zhang, Z. and N.W. Runham. – 1992. Otolith microstructure pattern in Oreochromis niloticus (L.). J. Fish. Biol., 40(3): 325-332. doi:10.1111/j.1095-8649.1992.tb02579.x; https://scientiamarina.revistas.csic.es/index.php/scientiamarina/article/view/1052

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    المؤلفون: Mérida Aguilera, Belén

    المساهمون: Morales Moreno, Aythami, Fiérrez, Julián, UAM. Departamento de Tecnología Electrónica y de las Comunicaciones

    المصدر: Biblos-e Archivo. Repositorio Institucional de la UAM
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    Relation: info:eu-repo/semantics/altIdentifier/url/https://www.jpeds.com/article/S0022-3476(18)31303-9/fulltext; http://hdl.handle.net/11336/125006; Cuestas, Eduardo; Aguilera, Belén; Cerutti, Manuel; Rizzotti, Alina; Sustained Neonatal Inflammation Is Associated with Poor Growth in Infants Born Very Preterm during the First Year of Life; Mosby-Elsevier; Journal of Pediatrics; 205; 2-2019; 91-97; CONICET Digital; CONICET