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<br />. <br /> <br />have replaced the Gila spinedace (Medafulgida), and exotic mosquito fish (Garn- <br />busia affinis) have replaced the Gila topminnow (Poeeiliopsis oeeidentalis oeci- <br />dentalis) in the Gila drainage. Mosquitofish also have replaced desert pupfish in <br />the Salton Sea, and exotic largemouth bass (Micropterus salmoides) and sailfin <br />mollies (Poecilia latipinna) have replaced Moapa dace (Moapa eoriaeea) and <br />White River springfish (Creniehthys baileyl) (Minckley & Deacon 1968; Minckley <br />1973; Deacon 1979). Minckley (1979) believes that the greatest impact is in <br />predation on juvenile natives, especially by juvenile exotics. In some cases, <br />hybridisation between native and exotic species has "swamped" the native gene <br />pool (e,g, rainbow X cut-throat trout: Behnke & Benson 1980). Further, range <br />restrictions and habitat change~, including the effects of exotic species, may be <br />enhanced by hybridisation between native species (e.g. razorback X flannel- <br />mouth sucker: Hubbs & Miller 1953; Tyus et al. 1982). <br />Exotics have been especially successful in reservoirs (Stanford & Ward 1986b) <br />and closely regulated segments (Stanford & Ward 1986a: Fig, 1). The major <br />fisheries in Lower Basin reservoirs involve the planktivorous threadfin shad, <br />which provides food for largemouth (Micropterus salmoides) and striped <br />bass (Morone saxatilis) (Dill 1944; Kimsey 1957; Minckley 1973). In Upper <br />Basin reservoirs a host of introduced suckers, minnows and trout are pre- <br />sent. Throughout the system, introduced fish have become established in the <br />remaining river segments through stocking or migration from the reservoirs <br />(Table 2). <br />The Serial Discontinuity Concept of Ward & Stanford (1983) - the idea that <br />regulated rivers tend to ecologically reset or mimic upstream or downstream <br />lotic conditions - predicts that native species should be re-established some <br />distance downstream from a dam, However, in the Colorado system there may <br />no longer be sufficient river lengths for this to occur, especially with the presence <br />of the exotic species, Big-river endemic species survive in the lower Green River <br />and the mains tern above Lake Powell because conditions approach pre-regulation <br />conditions, but even these segments are likely to be affected by dams proposed <br />or under construction on the lower reaches of the Yampa, White, Dolores and <br />Gunnison rivers, <br />I <br />; Productive exotic sport fisheries have been created below several dams: <br />growth rates of trout reportedly are more than 38--40 cm annually (Wiley & <br />Duffer 1980). Some fisheries have developed immediately below dams (e,g, Lee <br />Ferry fishery below Glen Canyon Dam), and others (e,g. lower Gunnison Rivcrl <br />are most productive some distance downstream from the dam, as cold tern. <br />peratures in the tailwaters are ameliorated by warm air temperatures and sid~' <br />flows (Stanford & Ward 1983, 1984). <br />A productive fishery developed in the Green River below Flaming Gorgt' <br />. Dam as the reservoir was filling (1962-68), but declined dramatically in respoTl'C <br />to cold (40C) releases after the reservoir filled (maximum depth 134m), In an <br />effort to salvage the fishery in 1978 the dam was fitted with multi-level relea'c <br /> <br />398 <br /> <br />~ <br /> <br />gates to allow a constant summer tailwater temperature of e. 130 C. Trout <br />growth increased 3--4 fold in the warmer water (Larson et al. 1980). <br />The Lee Ferry fishery below Lake Powell involves a simple food chain, and <br />produces fast-growing rainbow and other introduced trout (Plate Ig). The clear, <br />nutrient-laden water from the hypolimnion of Lake Powell stimulates growths of <br />the green alga Cladophora glomerata on the river bottom, sustaining high produc- <br />tion of introduced amphipods (Gammarus laeustris; see Ward et al. 1986), in <br />turn fed upon by trout. This fishery extends well into the Grand Canyon and is <br />a very different trophic system to the one that existed before impoundment. <br /> <br />Conclusion <br /> <br />The indigenous fish of the Colorado system have few marine affinities (Miller <br />1958) and are 85% endemic (66% at the species level), suggesting long isolation. <br />For some forms, however, survival may depend on artificial propagation <br />(Greger & Deacon 1982; Hammon & Inslee 1982), The system now is so altered <br />by regulation that questions about ecology of fish in the virgin river are largely <br />academic. Non-native species abound throughout, and the prospect for further <br />introductions is strong. Populations will likely fluctuate widely as interspecific <br />competition and the ecological consequences of regulation differentiate "winners <br />and losers". <br />Many research opportunities remain. Relationships between processes in <br />reservoirs and tail waters and successful fish populations are little understood. <br />The life histories and needs of forage organisms and factors controlling primary <br />productivity must be related to the fish communities, especially if sport species <br />are to be preferred, The regulated Colorado system provides experimental <br />macrocosms in which organism-level (e.g. gene expression) or ecosystem-level <br />(e.g. reservoir influences) theories may be tested (cf. Ward & Stanford 1984), <br />Answers to these questions may help to couple the benefits of regulation with <br />the natural attributes of the system. <br /> <br />Acknowledgements <br /> <br />We thank Dr R. Behnke and G. Wilde for reviewing the manuscript and R. <br />Valdez, J. Rinne, W. Dreyer, J. Johnson, C. Carlson, R. Harris and G. Bryant <br />for unpublished material. <br /> <br />References <br /> <br />Behnke, R. r 1981. Systematic and zoogeographical interpretation of Great Basin trouts. In R. J. <br />NallJ1an & D. L. Soltz (eds). FIshes in North AmerIcan Deserts. John Wiley & Sons, N,Y.: <br />95-124. ' <br /> <br />399 <br />