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<br />398 <br /> <br />The Southwestern Naturalist <br /> <br />vol. 38, no. 4 <br /> <br />opened, and the contents identified under a stereo <br />microscope. <br />A total of 466 fish was examined, including <br />184 red shiner (36-79 mm TL), 47 sand shiner <br />(30-65),42 fathead minnow (32-60), 176 redside <br />shiner (36-77), and 17 channel catfish (51-144). <br />Fish larvae were found in 15% of the red shiner, <br />always in the foregut region; no larvae were de- <br />tected in digestive tracts of other species. The <br />temporal distribution of fish larvae in red shiner <br />was as follows (parentheses show number of red <br />shiner examined, number with fish larvae, and <br />number of fish larvae per digestive tract): 30 June, <br />1600-1800 h (35, 13, 1-6); 2 July, 1200-1400 <br />h (20, 3, 2), 1600-1800 h (19, 2, 1-9), 2000- <br />2200 h (11, 7,1-7); 14 July, 1200-1400 h (6,1, <br />1),1600-1800 h (17, 2,1-3). One to 17 red shiner <br />(X = 5.1) were selected for examination from <br />collections made during the remaining sampling <br />times. <br />Of the 58 fish larvae found, most were too <br />digested for species identification or accurate <br />length measurements, but all were cypriniforms <br />(mostly catostomids) and probably S 15 mm TL. <br />Seven fish larvae, 11-13 mm TL, were identified <br />as bluehead sucker, five from red shiner collected <br />at 1600-1800 h on 30 June and one each from <br />red shiner collected at 1200-1400 hand 2000- <br />2200 h on 2 July. Insects, including adult or <br />immature caddisflies, mayflies, beetles, and water <br />striders, were the principal food items found in <br />digestive tracts of all fishes except fathead min- <br />now, which contained mostly algae and organic <br />debris. <br />Larval fishes were present in embayments dur- <br />ing each sampling period throughout our study. <br />Those collected and identified included roundtail <br />chub, speckled dace, and bluehead sucker. How- <br />ever, fish larvae were found only in red shiner <br />collected during daylight or dusk on 30 June and <br />2 and 14 July, and their frequency of occurrence <br />was 37% on 30 June, 20% on 2 July, and 8% on <br />14 July. Minckley (1973) reported that red shin- <br />er may be piscivorous, but we only found one <br />published account of this species eating fish lar- <br />vae. Jennings and Saiki (1990) reported that of <br />79 digestive tracts from red shiner collected in <br />the San Joaquin River drainage, only one con- <br />tained cypriniform larvae. <br />The high incidence of fish larvae ingested by <br />red shiner suggests that this species may be an <br />important predator on native fishes in the Col- <br />orado River system. Red ,>iner is one of the most <br /> <br />abundant and widespread nonnative fish species <br />in the system. Because red shiner occupy nursery <br />habitats used by young of native fishes, including <br />Colorado squawfish and razorback sucker, pre- <br />dation by red shiner may have a significant effect <br />on survival of larval fish. Also, red shiner has <br />been described as an opportunistic drift feeder <br />(Sublette, 1975), and therefore may prey on drift- <br />ing fish larvae. One possible explanation for fail- <br />ure of previous diet studies to produce evidence <br />of such predator-prey interactions in backwaters <br />is that preferred invertebrate forage was suffi- <br />ciently abundant to reduce the degree of piscivory <br />below detectable limits. Because water levels in <br />shoreline embayments fluctuate greatly with small <br />changes in river discharge (resulting in periods <br />of dewatering or flushing and substrate scouring <br />during flooding), abundance of invertebrate for- <br />age in this type of nursery habitat may be low, <br />especially in spring-early summer when changes <br />in river discharge are greatest and densities of <br />insects in low-velocity habitats are inherently <br />lower (L. W. Crist and S. D. Hiebert, U.S. Bu- <br />reau of Reclamation, pers. comm.). In laboratory <br />tests, presence of alternative invertebrate prey re- <br />duced the rate of predation on Colorado squaw- <br />fish and razorback sucker larvae by nonnative <br />fishes (R. T. Muth, pers. obser.). <br />Early larvae of Colorado squawfish were cap- <br />tured in the main channel of the Yampa River <br />at the upstream end of our study area during 7- <br />30 July 1991 (K. R. Bestgen, Colorado State <br />University, pers. comm.), but none was collected <br />in embayments we sampled. Our study began at <br />least a few weeks after the suspected spawning <br />season of razorback sucker in the upper Colorado <br />River system (April-June; Tyus and Karp, 1989). <br />Young razorback sucker produced at the lower <br />Yampa spawning site may have been transported <br />beyond our study area or were sufficiently large <br />(e.g., >20 mm TL; R. T. Muth, pers. obser.) to <br />avoid predation by smaller nonnative fishes. <br />However, if predation by red shiner on fish larvae <br />is in part a function of availability of alternative <br />prey, and if abundance of preferred invertebrate <br />forage is lower during spring and early summer <br />in at least some nursery habitats (e.g., shoreline <br />embayments), early larvae of razorback sucker <br />may be especially vulnerable. Effective assess- <br />ment of the extent and potential impacts of pre- <br />dation by nonnative fishes on larvae of native <br />fishes req uires better investigation of spatio-tem- <br />poral patterns in distribution and abundance of <br />fish larvae and invertebrate forage and the sea- <br /> <br />~ <br /> <br />liiI <br />.' <br />