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STOCK ASSESSMENT OF WHITE GRUNT FROM THE WEST ...

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Similarly, point estimates of annual mortality rate for white grunt caught in the head-boat<br />

fishery calculated using Robson and Chapman’s (1961) estimation procedure were 0.280 and<br />

0.303 for spawning and post-spawning females, respectively, and 0.376 and 0.375 for spawning<br />

and post-spawning males, respectively (Murie and Parkyn 1998). Hence total annual mortality<br />

for female grunts based on Robson and Chapman’s estimates were within the 95% confidence<br />

interval calculated using regression analysis, but for males the estimates based on Robson and<br />

Chapman’s method were slightly greater than the upper confidence limit of the catch-curve<br />

analysis.<br />

Manooch (1976) estimated mean total mortality for white grunts from North Carolina and<br />

South Carolina in the 1970’s to be between 37 and 51%, slightly greater than the total mortality<br />

range for white grunts in the Gulf in 1998 (range of 28 to 38 %). The catch curve that Manooch<br />

(1976) used to calculate total mortality for white grunts from the Carolinas was fundamentally<br />

different than the catch curve for white grunts in the Gulf of Mexico (Murie and Parkyn 1998).<br />

In particular with regard to total mortality estimates, Manooch (1976) did not have white grunts<br />

fully recruited into the head-boat fishery until they were age 7, and the oldest fish that was aged<br />

in his study was age 13.<br />

Both of the methods used to estimate survival rate, and hence mortality rate, of white<br />

grunts in the Gulf are based on the underlying assumptions that for the age classes in the<br />

analysis: 1) survival rate is uniform with age, and hence mortality rate is uniform with age; 2)<br />

mortality rate has not changed with time; 3) all ages represented in the analysis have been<br />

sampled randomly (i.e., they are equally vulnerable to the sampling gear); and 4) recruitment is<br />

constant for all year classes (Ricker 1975). It was readily apparent that white grunts may have<br />

undergone significant changes in recruitment among year classes. This was especially evident<br />

with age class 5, which was the 1993 year class, because it was poorly represented in both<br />

females and males. Although the mechanism(s) involved in producing a weak or strong year<br />

class are unknown and difficult to evaluate (i.e., spawning failure, differential recruitment,<br />

density-dependent mortality, etc.), trends in year class strengths can be effectively assessed<br />

through cohort survivorship curves by obtaining catch curves over a series of years or,<br />

alternatively, by a tag-recapture program (Robson and Chapman 1961, Krebs 1989).<br />

Annual estimates of average fishing mortality for white grunt (made using the modified<br />

DeLury models) peaked during the early to mid 1990s on both coasts. On the Atlantic coast,<br />

average instantaneous fishing mortalities peaked at 0.47-0.49 per year in 1992 then decreased<br />

through 1995 but has increased since (Fig. 24). The range of estimates for instantaneous fishing<br />

mortality in 1998 was 0.25-0.28 per year. On the Gulf coast, the peak in fishing mortality<br />

occurred in 1994 or 1995 when F reached about 0.30 per year (Fig. 24). Since then fishing<br />

mortality has declined reaching about 0.18 per year in 1998. Given an estimate of M equal to<br />

0.2 per year, the Murie and Parkyn (1998) estimate of total mortality would represent<br />

instantaneous fishing mortalities (F) ranging 0.08-0.23 per year for Gulf coast populations of<br />

white grunt. Similarly, the Manooch (1976) estimate of total mortality for the Atlantic coast<br />

grunt population would represent Fs ranging from 0.26-0.51 per year.<br />

The estimated average F relative to F MSY (fishing mortality at maximum sustainable<br />

yield) showed the same patterns seen for the absolute estimates of F (modified DeLury<br />

estimates). The estimated ratios of F/ F MSY are much more precise than are the absolute<br />

estimates of F made using the biomass dynamic model ASPIC (Prager 1994).<br />

15

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