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RfdNNESTAD AND FYHN REVIEWS IN FISHERIES SCIENCE <br />aspartic acid, glutamic acid, or taurine, dominate (Yancey et al., 1982; Pierce and <br />Politis, 1990). The pool size varies among groups; crustaceans have particularly high <br />cellular FAA levels. The FAA contents of marine invertebrate larvae have been <br />documented in some species, and the available data indicate that most have high <br />levels (see review by Fyhn E1990]). <br />Investigations during the last decade have shown that FAA also abound in <br />marine pelagic fish eggs (Suzuki and Suyama, 1983; Fyhn et al., 1987; Fyhn, 1989, <br />1990, 1993). The concentration in the egg (about 150 mrY~ is well above what is <br />typically found in adult teleostean tissues (Fugelli, 1970; Vislie, 1980, 1982). As was <br />the case in invertebrates, FAA in fish eggs were initially studied in order to evaluate <br />their role as osmolytes (12iis-Vestergard, 1982; Mangor Jensen et al., 1983; Mangor- <br />Jensen, 1986; H~lleland and Fyhn, 1986). More recently, however, FAA have been <br />implicated as a fuel in the energy metabolism of developing marine fish eggs and <br />larvae (Fyhn et al., 1987; Fyhn, 1989). The aggregate data from the literature, and <br />experiments on Atlantic cod (Gadus morhua) and Atlantic halibut (Hippoglossus <br />hippoglossus), suggested that the FAA were consumed as fuel during energy <br />metabolism of developing larvae (Fyhn, ,1989, 1990). In general, amino acids can <br />enter the tricarboxylic acid cycle to yield high energy nucleotide phosphates after <br />deamination. This bioenergetic hypothesis provided a new perspective for studies <br />regarding the FAA pool in developing marine fish eggs and larvae. <br />In the ocean, larval fish begin exogenous feeding on various planktonic <br />organisms that are, as mentioned earlier, rich in FAA. The developing fish larvae <br />thereby gain access to an entirely new and additional supply of FAA. Fyhn (1990) <br />argued that throughout 150 to 200 million years of teleost evolution in the oceans, <br />fish larvae may have become nutritionally adapted to this exogenous supply of FAA. <br />It also has been hypothesized that the amino acids consumed during the yolk-sac <br />stage reflected the nutritional needs of the larvae when converting to exogenous <br />feeding (Fyhn, 1989, 1990). That hypothesis gained much attention because it <br />deviated from the generally accepted thinking that lipids, especially the essential <br />highly unsaturated fatty acids (HUFA) of the n-3 and n-6 series were the key to <br />survival and growth of fish larvae at first feeding (Watanabe et al., 1983; Henderson <br />and Sargent, 1985). In fact, several studies have concluded that the principal factor <br />determining the dietary value of zooplankton is their n-3 HUFA content (Kitajima et <br />al., 1980; Watanabe et al., 1983; Walford and Lam, 1987; Izquierdo et al., 1989). In <br />contrast, the hypothesis suggested by Fyhn (1989, 1990, 1993) focused on amino <br />acids and the energy requirements of the developing larvae. <br />8. OBJECTIVES <br />In this review, the overall objective is to present the status of research regarding the <br />role of FAA in developing marine fish eggs and larvae. The principal focus is to <br />elucidate the metabolic aspects of FAA during fish ontogeny and to provide a <br />conceptual framework for catabolic and anabolic processes involving FAA. The <br />nonmetabolic aspects resulting from the physiochemical properties of FAA are not <br />discussed. <br />240 <br /> <br />