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150 <br /> <br /> v Low <br />100 L <br />rn <br />3 <br />0 E <br />50 <br />rn J.- <br />0 <br />2 4 6 8 <br />30 <br />v Low <br />E 25 ? Medium <br />E <br />O High 01 c: 20 <br />w f <br />- 15 <br />0 <br />o ?v? L <br />10 <br />FEEDING BY LARVAL RAZORBACK SUCKERS <br />0 2 4 6 8 <br />Week <br />FIGURE 3.-Mean weight (A) and mean total length <br />(B) of razorback suckers reared for 8 weeks in ponds <br />fertilized at low, medium, and high levels at Dexter Na- <br />tional Fish Hatchery, New Mexico, 1985. <br />There also were no differences among treat- <br />ments in selection of prey by taxon or size. Data <br />were therefore pooled for analysis of larval food <br />selection. First-feeding larvae selected rotifers and <br />tiny chironomids. Copepods and chironomids were <br />347 <br />eaten by intermediate-sized fish, and the largest <br />fish clearly selected cladocerans (Figure 7). These <br />taxonomic trends are primarily explained by prey <br />size (Figure 8). Small larvae selected animals 0.1 <br />mm or less in width (largely rotifers and chiron- <br />omids). As larvae grew, they shifted to copepods <br />(about 0.2 mm wide), and they ate organisms that <br />averaged 0.3 mm (mostly cladocerans) when 20.0 <br />mm TL or longer. From our data we do not know <br />whether organisms wider than 0.3 mm might have <br />been preferred by the larger larvae, because few <br />invertebrates in our ponds exceeded this size. Ra- <br />zorback sucker larvae may have selected the larg- <br />est organisms that were also most abundant. <br />Discussion <br />Addition of nutrients to an aquatic system tends <br />to increase density of primary producers and in- <br />vertebrates (Geiger 1983; Geiger et al. 1985; Pace <br />1986), which in turn may enhance food-related <br />survival and growth of fishes. Populations of algae <br />and invertebrate consumers increased rapidly in <br />our experimental ponds after fertilized and unfer- <br />tilized ponds were filled. Invertebrate populations <br />had broadly similar growth patterns in all ponds, <br />although they varied considerably in detail. Fer- <br />tilized ponds developed greater numbers and <br />biovolumes than did untreated ponds. Numbers <br />were positively correlated with fertilization rates, <br />but biovolumes in untreated ponds and those fer- <br />tilized at an intermediate level were similar and <br />lower than in highly fertilized ponds. Inverte- <br />brates were dominated by small-sized taxa, es- <br />pecially early in the experiment. Invertebrates had <br />greater size diversity when ponds were fertilized <br />than when they were not. <br />There were no significant differences in su ival <br />of larval razorback suckers in the various reat- <br />ments. Presence or absence of tiger salam nder <br />larvae, which can be both competitors of fis lar- <br />vae (Collins and Holomuzki 1984) and pred tors <br />TABLE 3.-Frequency of occurrence of various food items in stomachs of razorback sucker larvae during th? first <br />7 d after larvae were stocked into ponds. Frequency data include larvae with empty stomachs. <br /> <br />Week 1, day <br />Larvae (N) Frequency of occurrence (%) in stomachs <br />Phytoplanktona Diatoms Detritus <br />Otherb <br />Empty (' <br />Yo) <br />8 8 50 38 50 0 25 <br />9 10 30 50 50 20 50 <br />10 68 22 47 51 10 40 <br />12 30 25 67 80 63 17 <br />13 13 46 38 62 69 15 <br />14 43 23 49 51 88 5 <br />I Excludes diatoms. <br />b Includes rotifers, nauplii, cladocerans, invertebrate eggs, and chironomids