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INTRODUCTION <br />Background <br />Populations of Colorado squawfish (Ptychocheilus lucius) and razorback sucker (Xyrauchen <br />texanus) have diminished since historic times. The range of the Colorado squawfish has been <br />reduced by 80% (Tyus 1990); the razorback sucker, a similar amount. This has compelled the U.S. <br />Fish and Wildlife Service (USFWS) to list each as endangered species. Both species are endemic <br />to the Colorado River basin and were formerly widespread and abundant (Girard 1856, Jordan and <br />Evermann 1896, Miller 1961). Riverine populations are now confined to the upper basin (upstream <br />of Glen Canyon Dam). There, the Colorado, Green and San Juan rivers and associated tributaries <br />comprise the remaining range of these species. Currently, the Green/Yampa river system supports <br />the most viable population of Colorado squawfish and also contains the largest number of adult <br />razorback sucker remaining in the upper basin (Holden and Wick 1982, Lanigan and Tyus 1989). <br />The San Juan system contains the most diminutive population of Colorado squawfish, and no <br />razorback sucker have been found there in recent years (Ryden and Pfeifer 1993). This report <br />focuses on the Colorado River. There, a small remnant population of razorback sucker persisted <br />up through the mid-1980's; since then only a few individuals have been captured (Valdez et al. <br />1982, Osmundson and Kaeding 1991, Burdick 1992, USFWS unpublished data). Colorado squaw- <br />fish continue to persist but distribution and abundance have declined to the point that long-term <br />survival is far from assured. <br />Reduction in range can generally be attributed to dams and diversion structures. Large dams and <br />associated cold-water releases render downstream reaches uninhabitable. Range is also reduced <br />where large or small structures prevent young and adults from returning upstream after they have <br />migrated downstream. In those nonfragmented reaches where habitat for all life phases still exist, it <br />is difficult to quantify the factors that negatively effect remaining populations. Factors that have <br />been implicated include predation or competition from nonnative fishes, mortality from ingestion of <br />spined prey, angler-associated adult mortality, reproductive problems associated with environmen- <br />tal contaminants, low egg-hatching success due to infrequent flushing of spawning substrates, a <br />reduced food base, low availability of quality nursery habitat, and degradation or simplification of <br />adult habitats. Though some or all of these factors may act in concert, the relative importance of <br />each for each species within each river is unknown. Indeed, several of these factors are strongly <br />suspected but have not been demonstrated. <br />With the exception of angling mortality and problems associated with environmental contaminants, <br />many of the suspected problems listed above have been caused or exacerbated by flow regimes that <br />have been significantly altered during the past 100 years. Even problems associated with nonnative <br />fish can in part be linked to reduced flows that have allowed the colonization and continued <br />proliferation of certain species (Osmundson and Kaeding 1991, Muth and Nesler 1993). <br />Legal protection of sufficient instream flows to support self-sustaining populations of the endan- <br />gered fish is one of the primary goals of the Recovery Implementation Program' (USFWS 1987, <br />USFWS 1993). Instream flow needs are based upon the habitat requirements of rare fish species at <br />various life stages. Identification of habitat requirements and instream flow needs of the rare fish is <br />perhaps the most important element of the research effort expended by the Recovery Program.