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<br />968 <br /> <br />OSMUNDSON AND BURNHAM <br /> <br />be introduced, and floodplains may continue to <br />constrict from construction of additional jetties <br />and dikes and from further channel-stabilizing ef- <br />fects of exotic riparian vegetation (see Graf 1978). <br />Colorado squawfish, with their exceptional lon- <br />gevity (Osmundson et al. 1997) and high fecundity <br />(Hamman 1986), are well equipped to persist <br />through long periods of adverse conditions. His- <br />torically, their basinwide distribution no doubt <br />provided adequate colonization sources if drought <br />or other conditions temporarily rendered one or <br />more tributaries uninhabitable. Today, habitat <br />modifications occur rapidly and are likely to per- <br />sist for long periods; in addition, colonization <br />sources have been substantially reduced. Though <br />the nearby Green River population may serve as <br />a colonization source for the Colorado River (Gil- <br />pin 1993), a balance between local extinction and <br />colonization (see Gilpin and Hanski 1991) for this <br />and other wild populations is unlikely if extinction <br />is caused by a deterministic response to degraded <br />habitat conditions (Harrison 1991; Thomas 1994). <br />The same logic applies to stocking hatchery-reared <br />Colorado squawfish to reestablish extirpated pop- <br />ulations. Recovery to a viable, self-sustaining lev- <br />el depends on first identifying and then amelio- <br />rating or eliminating the ultimate limiting factors <br />(Tear et al. 1995). <br />For this population, a low frequency of strong <br />year-classes currently appears to limit adult abun- <br />dance. Although any increase in adult survival rate <br />would be beneficial, the success of recovery efforts <br />will largely depend on providing environmental <br />conditions that increase reproductive success and <br />survival of early life stages. <br /> <br />Acknowledgments <br /> <br />We thank Mike Tucker, Tom Fresquez, Dale Ry- <br />den, Mike Montagne, and Bruce Bonar for assist- <br />ing with data collection; Frank Pfeifer for admin- <br />istrative support; and Bob Burdick (USFWS) and <br />Bill Elmblad (CDOW) for sharing their respective <br />data sets. We appreciate Karl Seethaler, Rich Val- <br />dez, Chuck McAda, and Toby Mourning for al- <br />lowing our use of their length-frequency data from <br />1974 to 1976, 1979, 1982, and 1995, respectively. <br />Kevin Bestgen, Tom Chart, Bruce Haines, Pat <br />Martinez, Tom Nesler, Ron Ryel, Jack Stanford, <br />and an anonymous reviewer provided valuable <br />comments on various drafts. Ron Ryel also pro- <br />vided assistance with statistical analyses. Funding <br />was provided by the U.S. Fish and Wildlife Service <br />and the Recovery Implementation Program (RIP) <br />for Endangered Fish Species in the Upper Colo- <br /> <br />rado River Basin. The RIP is a joint effort of fed- <br />eral and state resource agencies, upper basin water <br />and power user groups, and environmental organ- <br />izations. <br /> <br />References <br /> <br />Akaike, H. 1973. Information theory as an extension of <br />the maximum likelihood principle. Pages 267-281 <br />in B. N. Petro v and F. Csaki, editors. Second inter- <br />national symposium on information theory. Aka- <br />demiai Kiado, Budapest, Hungary. <br />Anderson, D. R., K. P. Burnham, and G. C. White. 1994. <br />AIC model selection in over dispersed capture-re- <br />capture data. Ecology 75: 1780-1793. <br />Anderson, R. 0., and S. J. Gutreuter. 1983. Length, <br />weight, and structural indices. 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