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67 <br />energetic costs of searching for a dispersed food source may provide <br />an explanation for the differential growth. <br />At Dexter NFH, razorback suckers <12.0 mm TL positively selected <br />small organisms (rotifers and chironcmid larvae) 50.1 mm body width <br />and did not take larger potential foods. As larval fish grew, larger <br />Organisms (mainly cladocerans) were preferentially taken, until mean <br />size of animals ingested was 0.3 mm wide in fish of approximately 23.0 <br />mm TL. Prey of appropriate sizes to be ingested were generally <br />abundant in the ponds. There was little preference for taxa that <br />could not be explained by size and abundance combined. Selection of <br />most organisms was random (as measured by Strauss' Li), and even where <br />positive or negative selection was indicated, it was scarcely <br />significant (except for cladocerans, which were positively selected by <br />larger fish; Fig. 10). Seifert (1972) reported a similar diet of <br />first rotifers and later cladocerans for larval white sucker, but <br />noted an overall indiscriminate feeding behavior. Wild larval <br />razorback suckers in Lake Mohave ate cladocerans most abundantly, <br />along with rotifers and copepods (Marsh and Langhorst 1988). Larvae <br />of the related cui ui (Chasmistes bus) 12.0 to 28.0 mm TL ate <br />cladocerans (32% by n umbers) , chirona mid larvae (26%) and copepods <br />(20%) in the Truckee River, Nevada (Scoppettone et al. 1986). <br />Maximum size of ingested prey was smaller than the maximm <br />possible sizes predicted from measurements of lip length. This trend <br />has been reported by others (Arthur 1976; Gadomski and Boehlert 1984),