Laserfiche WebLink
<br />2 <br /> <br />I <br />I <br />I <br />I <br />I <br />I <br />I <br />I <br />I <br />I <br />I <br />I <br />I <br />I <br />I <br />I <br />I <br />I <br />I <br /> <br />Osmundson and Smith (1995) reported that reduced flows and habitat modification <br />have allowed nonnative species to proliferate. Currently, shoreline and backwater habitats <br />required by larval pikeminnow are dominated by several introduced fish species (McAda et <br />aI., 1994) and if competitors are abundant, risk of starvation may be high in spite of <br />optimal flow and temperature regimes. Because Colorado pikeminnow larvae did not co- <br />evolve with predator species, avoidance of predation was not an advantageous behavior <br />for this life stage. This suggests that larval pikeminnow may be vulnerable to exploitation <br />by introduced predators. Bestgen (1997) believed predation to be a significant cause of <br />mortality on larval Colorado pikeminnow. The abundance oflarval competitors and <br />predators are also probably correlated with environmentaVhabitat factors. Therefore, even <br />in years with optimal flow and temperature conditions, Colorado pikeminnow larval <br />survival and the resulting year-class strength may be very poor due to abundant <br />competitors and predators. It may be that pikeminnow larval survival is highest in years <br />with sub-optimal environmental conditions if those conditions reduce numbers of their <br />competitors and predators. <br /> <br />This study was designed to collect passively drifting fish larvae in the water <br />column over a five-year study period. At the time of collection, Colorado pikeminnow <br />larval were typically in a size range of 8 to 11 mm which back-calculated to between six <br />and 15 days post hatch. This size and age is very early in larval development and therefore <br />these collections do not represent year-class strength. However, it is believed that these <br />collections represent levels of success during the spawning, incubation and hatching life <br />stages and may be a prerequisite for development of strong year-classes. If correlations <br />are not found between larval abundance in the drift and end of season young-of-year <br />abundance, biological interactions are suggested as the primary regulator of year-class <br />strength. If so, this further suggests that environment variables that limit population size <br />of introduced species may provide the most promising mechanism to improve numbers of <br />young-of-year endangered fish. <br /> <br />Data were extracted from similar studies in Utah (Trammel and Chart, 1999a and <br />1999b), to gain a better understanding of relationships between flow regime variables on <br />production of larval Colorado pikeminnow and their downstream transport, and <br />survivorship in nursery habitat in Utah. This data is needed by the Colorado River <br />Recovery Program to assist in formulating a Biological Opinion on operations of the <br />Aspinall reservoirs. Comparable studies have been done on the Green River to assess <br />affects of Flaming Gorge Reservoir releases on reproduction and recruitment of Colorado <br />pikeminnow (Bestgen et al. 1998). This study has the following objectives: <br /> <br />1) To determine the relative abundance of Colorado pikeminnow larvae <br />produced by wild adults in the upper main stem Colorado River within <br />Colorado. <br /> <br />2) To determine the effect offlow manipulation and habitat availability upon <br />growing season and size of Colorado pikeminnow young-of-the-year as it <br />relates to potential over-winter survival. <br />