Some of the main characteristics are
Here alternatives 1 and 3 will be those investigated. Figure 5.1 shows the estimated selection patterns and figure 5.2 the estimated recruitment. Selection patterns are similar for both alternatives while recruitment in recent years is usually better according to alternative 3. (growth is less)
Figure 5.3 shows mean length at age according to alternative 1, excluding all length dependent mortality.
In alternatives 3 and 4 growth was estimated for every year with some
penalty on changes between adjacent years. (
in von
Bertalanffys model was always the same). The factor that multiplies
growth in weight is shown in table 5. It indicates
that since 1989 growth in weight has been 5-15% less than before. Growth was of course variable before 1989 so the interannual
variability of growth should be extended further back.
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Future simulations were done with recruitment at age 1 after 1999 set to 90 million individuals, which is below long time average according to the model. In alternative 3 the growth multiplier was set to 0.9 after 1998. The following figures show development of catch, catchable biomass, and fishing mortality of age 7, using F = 0.4 0.6 0.8 1 1.2 1.4 and 1.6 for fish fully recruited to the catch. The estimated selection pattern indicates that only really large haddock > 50-60 cm are fully recruited to the catch (figure 5.1).
Figures 5.4 to 5.7 show development of catch, catchable biomass and fishing mortality of age 7 haddock. Alternative 1 where growth is fixed indicates higher fishing mortality today than alternative 3 does. This is logical as in alternative 1 (fixed growth) the only way for the model to get reduced weight at age is to increase fishing mortality. For management purposes the results in alternatives 1 and 3 are though similar, as less growth as in alternative 3 will give lower values of F0.1 and Fmax. Looking at figur 5.2 10% more recruitment should have been used in alternative 3 than in alternative 1.
Figure 5.10 shows estimated yield per recruit according to altenative 1. Fmax is 0.5 and F0.1 0.32. Less growth will give lower values of Fmax and F0.1.
Figures 5.11 to 5.13 show then the catchable biomass, catch and fishing mortality of age 7 haddock using F = 0.5 after 1998.
5 shows the contribution of the objective function. Length distribution from the survey contribute 5% of the total objective function. It is possible that larger haddock is less available to the survey. In that case using logistic function as the selection curve for the survey could lead to overestimate of the mortality of larger haddock. The estimation done in alternative 3 was repeated without using length distributions in the survey, giving identical results.
Interesting aspect of table 5 is that mean length at age in survey and catch fit better in alternative 1 than in alternative 3 which is opposite to what would be expected.
In the original run with haddock all survey indices were in 5cm length group which split age 1 in 3 parts. This did not change much except in the estimate of the 1998 yearclass which was 30% higher in number. The reason for that was that it the mean length was less than average so unusually many fishes were between 7 and 12cm. The model then used that length group to lift the recruitment up but only the 1990 yearclass had comparable number of fishes so small.
Some additional work is planned on the haddock example.