Page View
Barry, Terence P.; Malison, Jeffrey A. (ed.) / Proceedings of PERCIS III, the Third International Percid Fish Symposium, University of Wisconsin, Madison, Wisconsin, U.S.A., July 20-24, 2003
(2004)
Lester, Nigel P.; Morgan, George
(Management) Biological reference points for management of walleye (Sander vitreus) fisheries, pp. 115-116
PDF (884.0 KB)
Page 115
BIOLOGICAL REFERENCE POINTS FOR MANAGEMENT OF WALLEYE (Sander vitreus) FISHERIES Nigel P. Lester, Harkness Laboratory of Fisheries Research, Ontario Ministry of Natural Resources, 300 Water St., Peterborough, Ontario K9J 8M5, Canada, nigel.lester@mnr.gov.on.ca, and George Morgan, Cooperative Freshwater Ecology Unit, Department of Biology, Laurentian University, 1222 Ramsey Lake Rd., Sudbury, Ontario P3E 2C6, Canada. Introduction. Walleye (Sander vitreus), the rmost popular sport fish in Ontario, are known to inhabit approximately 4000 lakes in the province. Management of this dispersed fishery is difficult because it is not economically feasible to monitor each lake. A practical alternative is a sampling approach in which data from a statistical sample of lakes are used to evaluate the state of the resource and decide whether a change in fishing regulations is needed to protect walleye from over-exploitation (Lester et al. 2003). This judgement requires that indicators from each lake be compared to reference values that specify the maximum (or minimum) level that must be sustained to safeguard the long-term productivity of a stock. These reference values, known as Biological Reference Points (BRP), are expected to vary among lakes depending on environmental characteristics that affect walleye carrying capacity and maximum intrinsic rate of increase. This paper describes a method of establishing MSY-based reference levels of total mortality rate and stock biomass for walleye. These reference points are interpreted as upper (mortality) and lower (biomass) limits. Methods. We used the classical Graham-Schaefer model of surplus production (Quinn and Deriso 1999) as a basis for calculating reference points. This model implies that as fishing mortality rate. (F) increases from zero, the equilibrium biomass (B) of a stock decreases linearly, starting at B.. (i.e., carrying capacity) and reaching zero when F = Fes, (i.e., maximum intrinsic rate of increase). Because yield equals F * B, this relationship produces a dome shaped yield curve with a maximum sustainable yield (MSY) described as MSY = Fmsy Bm,, where Fmjy = Fexi/2 and B,,sy = B.12. To estimate Fea we used a life history based model (Lester and Shuter in prep.) that assumes density-dependent growth and an optimum reproductive schedule (i.e., the age of maturation and the investment in egg production maximizes net reproductive rate). That model predicts the relationship between Fox,, M (natural mortality rate) and the degree of growth compensation (h,/ho) is: M -h where ho is growth rate (cm/yr) of the unexploited population (F = 0) , hi is growth rate of heavily exploited population (i.e., F = Fex,), L, is the size of a fish when it is recruited into the fishery. This model also implied, for walleye, M = hd(20 + 0.4ho). Observed variation in growth rate, combined with results from bioenergetics models, implied that ho is higher in warmer climates: ho = 5.63 (G - 0.7)0.67, where G is growing degree days above 5"C x 10-3, and that maximum growth rate (h,) is approximately 2.5 times the unexploited rate. Assuming hho = 2.5 and L4=30 cm, we calculated M and Fex,, for climatic conditions that span the province of Ontario. A reference point for total mortality rate was then calculated as: Z4., = M + FI,/2. We calculated the expected walleye biomass at MSY as Bmy = MSY/FmS3 , in which MSY was calculated from an empirical formula (Lester et al. 2002): MSY = 1.70 H093 TDS042 G' 86 Area where TDS is total dissolved solids (mg/l) and and H is average daily thermal-optical habitat area available for walleye during the summer (ha). H is calculated as H = Area PT zele where PT is area of the lake shallower than the thermocline, Zrel is relative Secchi depth: Zrei = z- _ Za.. is effective maximum depth (i.e., maximum depth of the lake or depth of the thermocline if the lake is thermally stratified) and s is a basin shape parameter typically having a value near 1. Results. Our model indicates that Fa,, is approximately 1.6 times M when the growth compensation ratio is 2.5, implying that Zmsy is approximately 2.6 times M (Figure 1). Across a climatic gradient of 1000 to 2400 GDD, M ranges from 0.12 to 0.34 and Z,,,y, ranges from 0.34 to 0.85. The implied exploitation rate at MSY ranges from 20% to 40%. Biomass at MSY depends on water clarity relative to lake depth, as well as nutrient levels. Examples in Figure 2 illustrate that B,.,), is very sensitive to water clarity, reaching maximum values 115
Copyright January 2004 University of Wisconsin Board of Regents.| For information on re-use see: http://digital.library.wisc.edu/1711.dl/Copyright




