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,4~ <br />December 1994 Horn et al.-Odonate predation on razorback sucker <br />In both experiments, numerous odonate nymphs <br />disappeared through mortality to unknown <br />sources, such as cannibalism, or in most cases <br />emergence. Shed exuviae and winged adults pro- <br />vided evidence of the latter. It is unknown when <br />losses occurred. <br />DISCUSSION-Odonate nymphs clearly are ca- <br />pable of destroying substantial numbers of larval <br />razorback sucker under experimental conditions. <br />Small larvae exposed to dragonfly nymph pre- <br />dation experienced only 24% survival and those <br />exposed to damselflies had 19% survival com- <br />pared to 88% survival in control aquaria. Larger <br />larvae had higher survival, but were still impacted <br />heavily (47% survival with predators present <br />compared to 82% survival of controls). Larger <br />larvae tended to remain in the water column, <br />where nymphs were only occasionally observed <br />to be swimming. In contrast, newly hatched ra- <br />zorback sucker larvae, which do not have a func- <br />tionally buoyant gas bladder (Minckley and Gus- <br />tafson, 1982), were incapable of sustained <br />swimming, and spent most of their time on the <br />aquarium bottom. Larvae in or on the substrate <br />would presumably be more vulnerable to pred- <br />atory odonates. Further, larger larvae in our ex- <br />periment appeared to react quicker to odonate <br />encounters than small larvae and often escaped. <br />Observations of odonate attacks on larvae sug- <br />gest that odonates randomly encounter larvae sit- <br />ting on the bottom, or as larvae swim within <br />reach. In the laboratory experiment, nymphs, al- <br />thoughoccasionally observed to swim in the water <br />column, were confined to the bottoms and sides <br />of aquaria. Many odonates climb among aquatic <br />vegetation and adopt an ambush strategy to cap- <br />ture prey (Corbet, 1963). Tramea, the large li- <br />belluide used in this experiment was the most <br />common nymph observed in backwaters of Lake <br />Mohave, and is commonly associated with veg- <br />etation. Extensive growth of sago pondweed (Pot- <br />¢mogeton ~iectinatus) and spiny naiad (N¢jas ma- <br />rina) in Lake Mohave backwaters may exacerbate <br />predation by nymphs on young razorback suckers <br />by allowing nymphs perches from which to am- <br />bush passing fish. <br />Historically, backwater habitats would have <br />provided ideal shelter for young larvae. The num- <br />ber, and species, of predatory fishes was low prior <br />to establishment of the tremendous variety of in- <br />troduced centrarchids, catfishes and minnows now <br />occupying the system. Much of the decline in <br />373 <br />native fish populations has been attributed to these <br />introduced fishes. Most aquatic insect taxa, on <br />the other hand, are native or ubiquitous in dis- <br />tribution, posing no new or novel threat to ra- <br />zorback sucker larvae. Within the backwaters <br />themselves we have not, however, quantified what <br />percentage of predation is from odonates versus <br />other predaceous insect taxa. <br />Under present conditions, isolated backwaters <br />of the lake favor thick growths of vegetation and <br />may permit insect populations such as odonates <br />to become extremely large. In addition, many of <br />these backwaters retain water throughout the year, <br />allowing predators with longer generation times <br />to enter the system, and allowing continued pres- <br />ence of short-lived predators. Prior to construc- <br />tion of the dams, river levels varied widely on a <br />seasonal basis, drying up or flushing out many <br />backwaters, thus limiting both growth of vege- <br />tation and densities of potential predatory insects. <br />Further, isolated backwaters do not have any fish- <br />es that might feed on odonates. Within Lake Mo- <br />have itself, odonate nymphs are uncommon. This <br />is probably a result of the lack of vegetation and <br />the presence of insectivorous fishes. <br />Based upon our observations of the potential <br />impacts of odonate nymphs and other insect pred- <br />ators, several new approaches are currently under <br />investigation to increase survivorship of larval <br />suckers in backwaters. New backwaters have been <br />selected that dry completely on a seasonal basis <br />because of fluctuating lake levels. Drying kills <br />back all macrophytes. Although macrophytes do <br />reappear every year, young fish get a 6 to 8 week <br />period of time when macrophytes are not present. <br />After this time fish are too large (50 mm) to be <br />captured by odonates or other predaceous insects <br />that utilize macrophytes for perches. In addition, <br />no nymphs, or other species, are able to over- <br />winter because of the dry substrate. Populations <br />of nymphs appear every spring following breed- <br />ing by adult odonates moving into the area. Small <br />odonates appear about the same time the fish are <br />stocked, but by the time these nymphs are large <br />enough to take fish, razorback sucker have out- <br />grown their stage of vulnerability. Finally, larval <br />razorback sucker are now raised to 20 mm TL <br />before being released to backwaters in an effort <br />to further reduce the potential for predation. In <br />1993, implementation of such measures resulted <br />in a survival rate of 25% for 20 mm TL razorback <br />sucker larvae versus 1% or less for eggs and newly <br />hatched larvae (M. Horn, pers. obser.). Fish <br />