<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-
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