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239 <br />0.9 <br />0.8 <br />0.7 <br />CO 0.6 <br />O <br />m 0.5 <br />Z 0.4 <br />0.3 <br />0.2 <br />0.1 <br />0.3- <br />0 0.3 m sec' <br />0.2 110 0.9msec' <br />C <br />1 0.1 <br />m <br />Z <br />? 0.3 m secs <br />®0.9msec' <br />X. texanus X. texanus G. cypha G. cypha <br />(hump removed) (hump removed) <br />Figure 3. Drag (Newtons) exhibited by body casts of X. tex- <br />anus and G. cypha in the experimental flume with water veloc- <br />ities of 0.3 and 0.9 to s-1. Casts without hump are the same as <br />those with hump except the hump has been removed by sand- <br />ing. <br />exactly proportional to a velocity-squared rela- <br />tionship when fish casts with humps and humps <br />removed were tested at velocities of 0.3 and <br />0.9 m s-1 (Figure 3). <br />Lift assessment <br />As expected, net lift varied greatly among the <br />objects tested, and there was no lift on the sphere. <br />A sphere is symmetrical; therefore the low pressure <br />on one side is offset by the low pressure on the <br />other side, thus, there should be no net force per- <br />pendicular to the flow (Denny 1988). Lift exhibited <br />by the fish casts was dependent on species, but <br />negative lift was unaffected by the presence of a <br />hump. The nuchal process did not have an influ- <br />ence on the downward forces related to body de- <br />sign (negative lift), as indicated by the lift force <br />values of X. texanus and G. cypha casts before and <br />after removal of the hump, both tested at 0.3 and <br />0.9 m s-1 (Figure 4; p > 0.05). A slightly negative <br />lift was produced by X. texanus; however, G. cypha <br />produced a substantial positive lift, especially with <br />higher water velocities (Figure 4). The different <br />morphologies of X. texanus and G. cypha no doubt <br />resulted in very different trends in lift performance. <br />In part, this disparity can be explained by the <br />noticeable asymmetry of G. cypha. A greater per- <br />centage of body volume is found above the dor- <br />soventral mid-point between the leading edge of <br />the rostrum and the tailing edge of the caudal <br />-0.1 <br />X. texanus X. texanus G. cypha G. cypha <br />(hump removed) (hump removed) <br />Figure 4. Lift (Newtons) exhibited by body casts of X. texanus <br />and G. cypha in the experimental flume with water velocities of <br />0.3 and 0.9 m s-1. Casts without hump are the same as those <br />with hump except the hump has been removed by sanding. <br />Positive values indicate an upward force and negative values, a <br />downward force. <br />peduncle, thus producing positive lift due to lower <br />pressure on the dorsal surface. <br />Prey morphology <br />Prey body depth at the nuchal hump was highly <br />correlated with body total length for both X. tex- <br />anus and G. cypha (r2 = 0.984, n = 119, <br />range = 67-559 mm TL; r2 = 0.986, n = 224, <br />range = 36.5-410 mm TL, respectively). A similar <br />relationship also existed for fishes without nuchal <br />humps, C. latipinnis and G. robusta (r2 = 0.985, <br />n = 148, range = 34-574 mm TL; r2 = 0.987, <br />n = 228, range = 39-447 mm TL, respectively; <br />Figures 5 and 6). However, the slopes of the fishes <br />without nuchal humps was less than that of the <br />fishes with enlarged nuchal humps, demonstrating <br />that fishes with nuchal humps increase in body <br />depth much earlier in development (Figures 5 and <br />6). <br />Predator mouth gape <br />The dorsoventral measurement of mouth gape in <br />P. lucius determined the largest size prey that <br />could be ingested. Predator mouth gape was cor- <br />related with total length (r2 = 0.911, n = 103, <br />range = 175-805 mm TL). <br />When predator mouth gapes and prey nuchal <br />region depths were considered together it is evident