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INSTREAM FLOWS TO ASSIST THE RECOVERY OF ENDANGERED FISHES 7
<br />1970. However, accurate annual population esti-
<br />mates, based on recovery of fish tagged in the
<br />earlier study, are biased by differential tag reten-
<br />tion, although the population clearly has re-
<br />mained "much less than 1,000" (Kenneth P. Burn-
<br />ham, Colorado State University, 1 June 1993
<br />letter to Tim Modde, U.S. Fish and Wildlife Serv-
<br />ice, Vernal, Utah). A few young razorback sucker
<br />have been collected in the Green River in recent
<br />years (e.g., three fish <415 mm in 1993; Tim
<br />Modde, personal communication), and the age
<br />structure of the few razorback sucker collected
<br />annually on the Colorado River has declined in
<br />recent years (Chuck McAda, U.S. Fish and Wild-
<br />life Service, Grand Junction, Colorado, personal
<br />communication). Thus, some recruitment of adult
<br />cohorts may be occurring in the Green and Colo-
<br />rado rivers, perhaps related to higher flows.
<br />Whether stable or declining, the population of
<br />razorback sucker in the Green-Yampa system
<br />probably has not exceeded more than 1,000 fish in
<br />the last 2 decades. Because most of the very few
<br />razorback sucker captured in the Upper Colorado
<br />River Basin are older fish, I conclude, as did Tyus
<br />(1991a), that very little recruitment of adult ra-
<br />zorback sucker has occurred since the 1960's.
<br />Razorback sucker have been observed spawn-
<br />ing or in spawning condition (ripe) during the
<br />rising limb of the spring runoff at temperatures
<br />5-100 C below (McAda and Wydoski 1980; Tyus
<br />1987) the experimentally observed optimum
<br />range (20-22° C) for reproduction (Inslee 1982;
<br />Hamman 1985; Marsh 1985). Razorback sucker
<br />were commonly (50 or more per year) collected in
<br />the 15-mile reach of the Colorado River in the
<br />early 1970's, mostly in a gravel pit connected to
<br />the river near Grand Junction, Colorado (McAda
<br />and Wydoski 1980; Valdez and Wick 1983). That
<br />gravel pit washed out in the 1984 spring flood of
<br />record, and only incidental captures were made
<br />subsequently (Osmundson and Kaeding 1991).
<br />However, in spring 1993, 67 razorback sucker
<br />were taken from another gravel pit (Etter Pond).
<br />One 20-year-old fish was collected, but the
<br />rest were 9 years old, corresponding to spawn
<br />during the 1984 flood, when the pond was last
<br />connected to the river (Chuck McAda, personal
<br />communication).
<br />In addition to their propensity to inhabit man-
<br />made gravel pits that are at least ephemerally
<br />connected to the river, razorback sucker are most
<br />often captured in low velocity habitats in the chan-
<br />nel (Fig. 2) and wetland ponds connected to the
<br />channel (McAda and Wydoski 1980; Tyus et al.
<br />1987). Bulkley and Pimentel (1983) showed
<br />that razorback sucker preferred temperatures of
<br />22-25° C in shuttle box experiments. In the pota-
<br />mon reaches of the Upper Colorado River Basin,
<br />shallow, backwater, and wetland habitats are typi-
<br />cally closer to the preferred temperatures than is
<br />the river channel, especially in the upstream
<br />reaches, where razorback sucker are most com-
<br />monly found. Indeed, Wick et al. (1983) showed
<br />that backwaters flooded by spring runoff on the
<br />Yampa River were significantly warmer than the
<br />channel, thereby offering more degree-days for
<br />maturation of spawning condition. Naturally
<br />functioning backwaters (i.e., not influenced by
<br />erratic, regulated flows) also contain food sources,
<br />such as zooplankton, invertebrates associated
<br />with macrophytes, and microbially rich detritus,
<br />needed to mediate growth of razorback sucker
<br />(Wick et al. 1982; Wick 1991).
<br />The reproductive bottleneck that is preventing
<br />recruitment of razorback sucker in the Upper
<br />Colorado River Basin is unknown. Clearly, these
<br />suckers prefer lacustrine-like environments, ow-
<br />ing to their proclivity for low velocity habitats,
<br />especially flooded gravel pits and wetlands, dur-
<br />ing high flows. River flow regulation, wetland
<br />revetments, diversion dams (which limit migra-
<br />tory pathways; see Fig. 1), and presence of abun-
<br />dant native and nonnative predators (also dis-
<br />cussed below with regard to similar influences on
<br />squawfish) may prohibit the fish from using back-
<br />waters and seasonally flooded wetlands in a man-
<br />ner that will allow recruitment to occur annually.
<br />Indeed, in Lake Mohave on the Lower Colorado
<br />River, where a large population of razorback
<br />sucker has persisted for many years but did not
<br />recruit in spite of apparent spawning success each
<br />year, the recruitment bottleneck was attributed to
<br />predation of larvae and early juveniles by nonna-
<br />tive minnows and sunfish (Marsh and Langhorst
<br />1988; Marsh and Minckley 1989; Papoulias and
<br />Minckley 1992). The recruitment bottleneck for
<br />razorback sucker in the Upper Colorado River
<br />Basin very likely relates to the current paucity of
<br />low velocity, warm, food-rich, and nonpredator-
<br />dominated habitats during spring and summer.
<br />Instream flow recommendations are based pre-
<br />dominantly on ecological knowledge of Colorado
<br />River squawfish, which are the most abundant
<br />and best known of the endangered big river en-
<br />demics. Squawfish occur most abundantly in the
<br />potamon reaches of the Yampa, Green, White,
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