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<br />1376 <br /> <br />negative coefficient for the quadratic term forced the <br />relationship to decline for large fish. We hypothesize <br />that relatively small or very large fish are more difficult <br />to capture because of habitat use or behavioral <br />differences. Small fish can occupy relatively shallow <br />water or small backwaters, where accessibility by <br />electrofishing boats is limited (Tyus and Haines 1991). <br />Large fish may occupy particularly deep water where <br />electrofishing is simply inefficient or may be powerful <br />enough to evade the electrofishing field when it is <br />detected, While it is possible that there were more <br />small fish in the system than our abundance estimates <br />suggest, it is unrealistic to speculate that large numbers <br />of very large and old individuals went undetected by <br />our sampling efforts. Thus, we believe that low capture <br />probabilities for large adults have caused negligible <br />bias of abundance estimates for adult Colorado pike- <br />minnow. <br /> <br />Transition Rates <br /> <br />Transition probabilities reflected a general upstream <br />movement pattern for relatively small Colorado pike- <br />minnow from the lower Green River and the <br />Desolation-Gray Canyon reaches. This is consistent <br />with the size structure information presented here and <br />elsewhere, which shows relatively high abundances of <br />small Colorado pikeminnow in those reaches, includ- <br />ing recruits, compared with other reaches (Tyus 1991). <br />This pattem was also consistent with that in the <br />Colorado River, where relatively small-bodied Colo- <br />rado pikeminnow reared in lower sections of the river <br />and eventually moved upstream as subadults or adults <br />(Osmundson et al. 1998). The prevailing wisdom <br />suggests that recruit-size Colorado pikeminnow and <br />smaller juveniles in downstream portions of the Green <br />River basin would also generally move into upstream <br />areas and establish home ranges (e.g., Irving and <br />Modde 2000). Net movement was neutral or negative <br />to . upstream reaches such as the Yampa and White <br />rivers, however. Perhaps drought or other conditions <br />forced fish to move from relatively small upstream <br />reaches to larger ones such as the middle Green River, <br />a reach where the net annual Wi was positive. <br />Additional empirical analysis of the growth and <br />movements of Colorado pikeminnow based on tag <br />recaptures would also be useful to further understand- <br />ing of the ecology of Colorado pikeminnow in the <br />Green River basin, as was demonstrated by Osmund- <br />son et al. (1997, 1998). <br /> <br />Applications <br /> <br />This study has demonstrated that the use of <br />coordinated multiple-pass, capture-recapture sampling <br />to obtain reliable abundance estimates for fish in large <br /> <br />BESTGEN ET AL. <br /> <br />drainage basins is logistically possible and can <br />successful even when some reaches are in remote <br />white-water canyons. Future efforts to obtain abun- <br />dance estimates to address recovery goals for Colorado <br />pikeminnow should follow a similar approach. Sam- <br />pling for Colorado pikeminnow should also continue to <br />focus on high-density areas that support the majority of <br />the Green River population. In river reaches where <br />relatively few Colorado pikeminnow reside, increased <br />sampling efficiency is needed to improve the precision <br />of abundance estimates. <br />This study illustrates the complexity of the abun- <br />dance dynamics of big-river fishes like Colorado <br />pikeminnow that are long-lived and provides further <br />insights into the multitude of factors that affect them. In <br />our study, the abundance of adult Colorado pike- <br />minnow declined because of reduced survival and <br />recruitment. However, it was difficult to ascertain <br />whether the reductions were from anthropogenic or <br />natural causes or some combination of the two. <br />Recruitment of young to the adult life stage requires <br />several years, and recruit abundance may be affected <br />by flow regulation from upstream Flaming Gorge Dam, <br />habitat quality and availability, stochastic events such <br />as floods or drought, the interacting effects of abiotic <br />factors and predation, and other factors (Haines and <br />Tyus 1990; Tyus and Haines 1991; Bestgen 1996; <br />Bestgen et al. 2006a). Several of those factors may be <br />responsible for the changes in the abundance of adults <br />since 1991, which showed a large apparent increase in <br />population size up to 2000 but then declined. The <br />reductions in the abundance and survival of adult and <br />recruit -size Colorado pikeminnow in the Green River <br />basin may also be related to low, drought-related base <br />flows that began about the same time as this <br />investigation or to the increased distribution and <br />abundance of nonnative predaceous fishes. Thus, <br />although it is difficult to determine what specific <br />factors have caused Colorado pikeminnow populations <br />to fluctuate since the early 1990s, a better understand- <br />ing of the mechanisms underlying their abundance and <br />survival is needed to prevent future declines. <br />The results presented here also suggest that the <br />demographic parameters for endangered Colorado <br />pikeminnow do not meet recovery goal criteria for <br />downlisting or delisting at the present time (U.S. Fish <br />and Wildlife Service 2002). The Green River basin <br />criteria require relatively stable abundance over a 12- <br />year or longer period, with recruitment sufficient to <br />maintain a minimum of 2,600 adults. The recovery <br />goals also require, among other things, the provision of <br />adequate habitat and the reduction of other threats <br />(U.S. Fish and Wildlife Service 2002; Valdez and <br />Muth 2005). This work has begun with the reregulation <br /> <br />. <br />