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<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
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