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<br />~. <br /> <br />. <br /> <br />~~ <br /> <br />~ <br />~ <br /> <br />j <br /> <br />. <br /> <br />~ <br /> <br /> <br />and Wisby (1951). 1hey suggested that young salmon imprint to the odor of <br />their natal tributary, store this information in a long-term olfactory <br />memory, and later use this memory to relocate the stream during spawning <br />migrations. In the following 40 years, many other workers have tested and <br />further refined this hypothesis. It is now recognized that fish imprint to a <br />"home-site olfactory bouquet" which consists of environmental odors that may <br />include both a geologic and species-specific component (Hasler and Scholz <br />I983, foster I985). However, our knowledge of the adaptive significance of <br />migrations and reproductive cycles is poor for all but a few, commercially <br />important species. <br /> <br />Migration patterns of adult Colorado squawfish are similar year to year. <br />These movements are presumably an orientation to environmental conditions in <br />the spawning reaches, and movements of fishes in up- and downstream directions <br />is suggestive of an olfactory orientation mechanism (Harden-Jones 1968, Hasler <br />and Scholz 1983). Some behaviors associated with olfactory orientation in <br />sa1monids were exhibited by Colorado squawfish, and the presence of spring-fed <br />tributaries and other water inputs in spawning reaches may provide piloting <br />cues. Tributa~ streams m~ provide 9ross cues for long-distance orientation, <br />while more subtle cues, unique to specific sites, may be used for egg <br />deposition (Tyus, In press). Reproductive by-products from previously-hatched <br />young (foster 1985) may also be included in a home-site olfactory bouquet. <br />Colorado squawfish larvae may imprint such odors in the areas in which they <br />develop, and later recognize these odors as migrating adults. <br /> <br />Recaptured and radiota9ged adult Colorado squawfish have demonstrated a <br />fidelity (repeated return) to the same spawning areas (Wick et a1. 1983, Tyus <br />1985, in press). However, it has yet to be shown that these fish return to <br />natal areas for spawning. 1he similarity of their behavior to that of many <br />other fishes makes it probable that they do so, and this could lead to <br />reproductive isolation and separate genetic stocks. It is noted that the <br />maintenance of discreet stocks can be developed through spawning site <br />imprintin9 and homin9 (Horra11 1981), and thus, specific mi9ration routes and <br />positive or negative rheotaxis in homing orientation su9gests different <br />genetic stocks (reviewed by Smith 1985). Some genetic interchange between <br />stocks may occur from fish that "str~' from one area to another, and could be <br />important for successful evolution of the species (8aker 1982; Leggett 1984). <br />It is therefore important t~at the genetic identity of separate stocks of <br />Colorado squawfish be identified and protected. <br /> <br />Knowledge of the reproductive ecology of the razorback sucker is poorly <br />known, principally because successful recruitment is 1ackin9 throughout the <br />Colorado River Basin (Lanigan and 1yus 1989, Marsh and Minckley 1989). <br />However, razorback sucker migrations have been documented, and there is <br />compelling evidence that homing behavior occurs as in the white sucker. The <br />possibility of at least two separate spawning stocks of the razorback sucker <br />in the Green River basin (Tyus and Karp 1990) suggests that imprinting and <br />home site selection may be also be important considerations in the recovery of <br />this fish. <br /> <br />S1UDY ME1HODS AND APPROACH: <br /> <br />Because of the time required to do this work, and the critical need to <br />demonstrate progress towards recovery of endangered Colorado River fishes, we <br /> <br />12 <br /> <br />. <br />