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6.3. Applications with length covariate

The importance of fish length to migration rate has been analyzed in several studies (Brett, Hollands, and Alderdice, 1958; Washington, 1982). Longer fish are generally more mature (in terms of age and smoltification) and are expected to migrate at a faster rate than shorter fish. As a first application of the procedure, I compare the null hypothesis that ri is constant within a cohort to the alternative hypothesis that ri is linearly related to fish length. In other words, For each cohort, likelihoods, l0 and lA, are computed for the null and alternative hypotheses respectively. Comparing these two likelihoods yields an assessment of the performance of the two models relative to each other. With a likelihood ratio test, the null hypothesis is rejected at the 0.05 level if the ratio is greater than 21(0.05) = 3.84. Using Akaike's information criterion (AIC) the null model is rejected if the ratio is greater than 2.0. Using the Bayesian information criterion (BIC), the null model is rejected if the BIC for the length model (BICl) is greater than the BIC for the null model (BIC0), and I report the value BICl - BIC0. I will use these values as a rough measures of the relative performance of the two models.

Three sets of cohorts are analyzed in this section. The first two sets are Snake River spring chinook and steelhead analyzed in previous chapters. The third set is the mid-Columbia fall chinook.

results

The results of the analysis of the 3 data sets are contained in Table 6.1 - Table 6.5. These tables provide averages and standard deviations of length for each release group. Also contained in the tables are parameter estimates for the length model as well as log likelihoods for the null and alternative models, the ratios between the two, and the BIC values.

There is some support for the length model in the Snake River chinook cohorts (Table 6.1 and Table 6.2). Nine out of the 18 cohorts had likelihood ratios greater than 2.0, which is the AIC value at which the null hypothesis is rejected, but the null model is only rejected for five out of 18 cases based on the BIC values. The parameter estimate results are somewhat contrary to what I expected, however. In 14 out of 18 cohorts, is negative, indicating that the model predicts increasing migration rate for decreasing fish lengths. This is also true for 8 out of the 9 cohorts that had likelihoods ratios greater than 2.0.

Table 6.1 Results from the application of the individual covariate travel time model with length covariate to cohorts of Snake River "run-of-the-river" chinook. Note that a negative BIC value lends support to the null model (that is, the model without the length covariate).
cohort # # of fish length parameter estimates likelihoods
mean s.d. 0 1 l0 lA ratio BIC
1989
1 55 128.25 9.28 3.61 -0.006 4.42 -177.51 -177.44 0.15 -3.86
2 57 128.18 10.51 4.99 -0.015 7.02 -199.30 -199.07 0.46 -3.58
3 43 128.21 12.47 10.42 -0.056 7.26 -148.90 -147.10 3.60 -0.16
4 64 134.77 12.06 15.49 -0.059 9.97 -159.53 -158.50 2.06 -2.10
5 69 126.26 18.92 12.81 -0.036 8.34 -156.14 -154.79 2.70 -1.53
6 66 124.61 18.06 9.53 -0.016 7.75 -152.75 -152.46 0.59 -3.60
7 64 115.88 17.39 4.16 0.030 11.26 -164.28 -163.75 1.04 -3.12
1990
1 54 115.07 13.02 16.86 -0.069 7.83 -114.29 -112.20 4.17 0.18
2 66 118.95 14.24 15.49 -0.077 10.07 -182.78 -179.99 5.58 1.39
3 52 117.13 15.14 9.54 -0.028 5.90 -122.53 -121.38 2.29 -1.66

Table 6.2 Results from the application of the individual covariate travel time model with length covariate to cohorts of Snake River "run-of-the-river" chinook. Note that a negative BIC value lends support to the null model (that is, the model without the length covariate).
cohort # # of fish length parameter estimates likelihoods
mean s.d. 0 1 l0 lA ratio BIC
1991
1 55 124.22 12.06 4.00 -0.009 4.82 -178.31 -178.14 0.33 -3.67
2 66 128.32 9.84 9.03 -0.039 6.02 -197.19 -195.71 2.97 -1.22
3 51 127.88 10.16 5.61 0.004 8.35 -135.23 -135.22 0.01 -3.92
1992
1 50 130.00 9.32 8.14 -0.032 5.51 -147.50 -146.59 1.82 -2.10
1993
1 60 127.08 10.77 1.67 0.015 5.18 -182.64 -182.25 0.79 -3.31
2 46 123.72 11.22 10.29 -0.047 4.54 -124.04 -120.45 7.18 3.35
3 64 120.33 13.07 3.21 0.041 6.92 -135.87 -134.53 2.68 -1.48
4 57 122.02 10.87 12.48 -0.009 7.41 -95.49 -95.47 0.04 -4.00
5 74 121.14 18.26 -4.94 0.148 15.13 -154.11 -148.98 10.27 5.97

The results for the steelhead (Table 6.3 and Table 6.4) are similar to the Snake River chinook results. Five out of the 19 cohorts had likelihood ratios greater than 2.0, and three out 19 has positive BIC values, supporting the null model in most cases. Also, eight out of 19 had negative values for .

Table 6.3 Results from the application of the individual covariate travel time model with length covariate to cohorts of Snake River steelhead. Note that a negative BIC value lends support to the null model (that is, the model without the length covariate).
cohort # # of fish length parameter estimates likelihoods
mean s.d. 0 1 l0 lA ratio BIC
1989
1 64 185.89 29.98 27.94 -0.042 12.62 -84.61 -83.51 2.20 -1.96
2 79 182.48 20.62 8.13 0.058 17.19 -126.17 -125.68 0.97 -3.40
3 47 168.94 17.28 18.66 -0.019 11.69 -90.22 -90.16 0.11 -3.74
1990
1 61 182.57 23.54 -0.011 9.93 -101.38 -101.30 0.17 -3.94
2 95 176.74 14.80 0.67 0.067 6.84 -158.91 -154.53 8.76 4.21
3 146 171.97 16.02 8.33 0.021 12.01 -287.36 -287.11 0.50 -4.49
4 68 173.94 16.79 6.42 0.015 13.98 -168.08 -168.02 0.11 -4.10
5 61 169.43 17.40 11.38 -0.014 8.22 -128.11 -127.93 0.35 -3.76

Table 6.4 Results from the application of the individual covariate travel time model with length covariate to cohorts of Snake River steelhead. Note that a negative BIC value lends support to the null model (that is, the model without the length covariate).
cohort # # of fish length parameter estimates likelihoods
mean s.d. 0 1 l0 lA ratio BIC
1991
1 50 181.12 16.12 6.17 0.023 7.15 -89.39 -89.07 0.64 -3.27
2 126 178.67 15.29 24.78 -0.055 10.62 -201.54 -199.96 3.15 -1.69
3 56 173.95 16.23 13.99 -0.005 9.45 -94.36 -94.35 0.02 -4.01
4 51 165.82 17.33 11.55 0.050 12.75 -68.50 -68.23 0.54 -3.39
1992
1 67 181.40 17.63 8.21 0.011 6.40 -114.00 -113.84 0.31 -3.89
2 154 176.60 17.70 17.05 -0.014 10.23 -245.01 -244.83 0.36 -4.68
3 90 171.41 14.71 15.14 -0.038 7.34 -214.97 -213.39 3.15 -1.35
1993
1 50 178.28 21.30 7.47 0.032 10.85 -88.79 -88.35 0.88 -3.03
2 87 177.00 20.10 -3.21 0.114 9.44 -123.06 -115.73 14.66 10.19
3 59 173.93 19.03 -13.20 0.183 17.88 -100.69 -97.86 5.66 1.59
4 40 175.38 16.32 10.32 0.032 12.18 -64.90 -64.77 0.26 -3.43

Although the length covariate appears to have some importance in the travel time model for these two groups, it would be difficult to implement the length model based on these data because of the variability in parameter estimates. More information will be required to understand why the relationship between migration rate and fish length is sometimes positive and sometimes negative.

The results for the mid-Columbia fall chinook (Table 6.5) strongly support the inclusion of the length covariate in the travel time model. All the BIC values are positive, with 4 out 5 values greater than 10.0. Also there is consistency in the values of and , with most estimates of in the 3.0 - 5.0 range and most estimates of in the 0.10 to 0.14 range. Thus, including length information in the travel time model for these fish would be quite useful.

Table 6.5 Results from the application of the individual covariate travel time model with length covariate to cohorts of mid Columbia fall chinook. Note that a negative BIC value lends support to the null model (that is, the model without the length covariate).
cohort # # of fish length parameter estimates likelihoods
mean s.d. 0 1 l0 lA ratio BIC
1991
2 97 63.32 4.38 -0.60 0.062 6.86 -393.05 -390.38 5.33 0.76
1992
1 75 71.37 7.16 -5.11 0.125 5.58 -288.71 -264.16 49.11 44.79
4 63 69.00 7.21 -3.64 0.102 4.60 -239.05 -219.76 38.57 34.43
1993
1 61 66.80 6.49 -5.36 0.145 3.99 -222.15 -195.54 53.21 49.10
3 115 66.20 5.46 -4.96 0.134 5.92 -425.60 -404.48 42.24 37.50

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Spatial and Temporal Models of Migrating Juvenile Salmon with Applications.
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