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<br />250-700 V (2.4-6.7 peak V/cm). They also demonstrated a significant positive relationship <br />between mortality and exposure duration at 400 V but not at 250, 550, or 700 V. Dwyer <br />and Erdahl (1995) concluded that voltage level is more critical to mortality of cutthroat trout <br />eggs than either waveform or pulse rate. We found inverse relationships between mean <br />percent survival of razorback sucker embryos and both voltage gradient and pulse rate. <br />Survival of embryos shocked at early tailbud or finfold was significantly greater in the 30-Hz <br />(1.2-V/cm) treatment compared to the 80-Hz (1.2-V/cm) treatment, but effects of pulse <br />duration (4-ms pulses at 30 Hz and 5-ms pulses at 80 Hz) could not be evaluated with our <br />study design. <br />Our results and those of other studies suggest that fish embryos are most <br />susceptible to electro-shock mortality during the period from early cleavage through end of <br />epiboly (Le., when the blastoderm has overgrown the yolk, near beginning of the eyed <br />stage). This is a critical period of cell division and morphogenesis (Long 1984). <br />Mechanisms (physiological reactions or physical damage) responsible for increased <br />mortality in early embryos exposed to electric currents are unknown. However, Dwyer et al. <br />(1993) compared effects of electrical and mechanical shock on developing rainbow trout <br />embryos and found that ontogenetic patterns in sensitivity to either type of shock were <br />similar. Hayes (1949) and Post et al. (1974) reported that salmonid embryos are most <br />sensitive to mechanical shock during the early to mid-epiboly stage. Hayes (1949) <br />suggested that mortality induced by mechanical shock was due to rupturing of the vitelline <br />membrane. <br />Reduced growth of razorback sucker larvae exposed to electrofishing fields in the <br />wild could lower their chances of survival. Miller et al. (1988) and Rice et al. (1993) <br />suggested that lower mean growth rates of fish early in life can cause reduced survival by <br />prolonging the period of vulnerability to starvation and predation. Starvation and predation <br />by nonnative fishes have been hypothesized as factors limiting survival of razorback sucker <br />larvae, and existing evidence suggests that predation is a significant cause of larval <br />mortality (Minckley 1983; Marsh and Langhorst 1988; Minckley et al. 1991). <br />Survival of fish in early life stages often determines year-class strength of <br />populations. Houde (1987) reported that relatively minor variations in survival, growth, or <br />developmental rate of fish early life stages can cause substantial fluctuations in recruitment <br />success. Muth and Ruppert (in press) found that exposure of ripe razorback sucker to <br />homogeneous, square-wave 60-Hz (24% duty cycle) or CPS currents at 1.0 peak V/cm for <br />10 s injured fish, caused premature expulsion of gametes, and significantly reduced egg <br />hatching success. Results of this study suggest that electrofishing of razorback sucker <br />spawning aggregations could significantly harm embryos and early larvae, and in doing so <br />possibly further limit recruitment. Results support the recommendation by Muth and <br />Ruppert (in press) that the need for electrofishing over active razorback sucker spawning <br />areas should be carefully evaluated. <br /> <br />References <br /> <br />Bozek, M. A., L. J. Paulson, and J. E. Deacon. 1984. Factors affecting reproductive <br />success of bonytail chubs and razorback suckers in Lake Mohave. Final report. <br />U.S. Bureau of Reclamation, 14-16-0002-81-251, Boulder City, Nevada. <br /> <br />13 <br />