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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.
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