1.
2) CV combinations: for each survey using q age-aggregating from 1) fit all combinations (pooled and unpooled; see Supplementary Materials 1 for details) of CV ages while keeping one CV parameter for other two surveys. Survey CV formulations for each survey selected from run with lowest BIC.
3) re-check q: with survey CVs from 2), re-run 1) to check that q age-aggregation is the same as in 1)
4) crl sd ages: with survey CVs from 2) and q from 1), fit all combinations of crl sd ages. crl sd age formulation selected from run with lowest BIC.
5) crl sd years: with q from 1), survey CVs from 2), and crl sd ages from 4), fit two scenarios:
a. pre/post moratorium split: fit a separate age sd parameter pre/post moratorium for year split start ∈ (1990, 1999)
b. moratorium gap: fit one separate sd parameter (no age splitting) for 10-year mortarium gap for year gap start ∈ (1990, 1999).
crl sd year formulation selected from run with lowest BIC from both a and b
6) re-check q: with survey CVs from 2), crl sd ages and years from 4–5, re-do 1) to check that q age-aggregation is the same as in 1)
The best fitting model was selected from step 6 for each of the four runs (i.e. one best fitting model for runs S1-S4 selected via lowest BIC from step 6) and model fit compared across all four via a detailed examination of model residuals and BIC. Evidence of patterns in residuals (i.e. blocks of ages and years having residuals of the same sign, and whether or not overall residual variability matches assumption) was used to evaluate potential model mis-specification. The survey and continuation ratio logit residuals, which are correlated in our observation models, were standardized using the Choleski factorization of their estimated covariance matrix. We did not use the one-step ahead residual method (see e.g. Thygesen et al., 2017) because it does not allow for correlations in the observations. A final model was selected from the four S1–S4 best fitting runs (i.e. via BIC and residual fits) and in the final step, two extra runs were fit; one with all ϕ F parameters freely estimated and all ϕ C fixed and one with all AR(1) parameters freely estimated (O2). These two runs were compared to the run with the fixed AR(1) parameters (O1), and a final model selected from the three. In all subsequent text, SSM will refer to the final model.
The SSM fit was also assessed through retrospective model fitting for the years 2011–2017. Each retrospective model fit used one less year of data (i.e. model for year 2011 used data up to 2011) and predicted abundance, biomass, spawning stock biomass and average F’s were examined for systematic patterns and the severity of retrospective pattern was assessed using Mohn’s rho (see Mohn, 1999). Ideally, no discernable directional patterns will be present in the retrospective plots.
Biomass-at-age was calculated by multiplying predicted numbers at age (i.e. N y,a) and stock weights-at-age, which were estimated externally via a spatiotemporal biphasic Von Bertalanffy growth model (see Kumar et al., 2020). Length and age data are collected for American plaice from research survey vessels using a length-stratified age sampling design and Perreaultet al. (2019) showed that ignoring this sampling design can lead to biased growth model parameter estimates. Kumar et al.’s method (2020) accounted for the length-stratified age sampling design. The 3LNO stock weights were combined for each division by weighting the values for each division by the average abundance index at age during 1975–2017. Stock weights prior to 1975 were fixed at the mean values for 1975–77. Estimates of maturity-at-age were taken from Wheeland et al.(2018).
Simulation and sensitivity testing
A full simulation study is beyond the scope of this paper; however, we conducted a simple self-simulation test and jittered start on the SSM to examine the reliability of the model estimates see e.g. Cadigan, 2015; Nielsen and Berg, 2014). The self-simulation test randomly generates survey indices and continuation ratio logit catch proportions from the model predictions and assumed distributions detailed above. Process errors and other random effects are treated as fixed when generating the data and the model is re-fitted to the simulated data. This process is repeated 1000 times and estimates of SSB, average fishing mortality rates (ages 9–14), recruitment, variance and autocorrelation parameters are stored. We calculated the relative difference of the estimates for each year (i.e. (simulation SSBydata-based SSBy)/ data-based SSBy) for comparison.
The jittered start test re-fits the model with random noise added to the starting parameter values, generated from N(0,0.25 ∙ ˆ μ ), where ˆ μ is the model predicted parameter of interest. The model is re-optimized 100 times and the negative log-likelihood is stored for each iteration. Ideally, we expect an identical model fit from the jittered starting parameter values.
We also examined the model sensitivity to our assumptions about M and catch bounds. A profile likelihood was constructed for a range of M a,yʼs; that is, M a,y = M + ΔM, where M is the SSM M model formulation and ΔM ∈ ( − 0.1, 0.35). We also re-fit the model with upper catch bounds fixed at half the original model formulation upper bounds (M2) and with the upper catch bounds fixed (M3) at 1% of the reported bounds (i.e. “fixed landings”). Model fit for the catch bounds was assessed using BIC and an examination of the retrospective plots.
Results
For brevity, we provide a summary table of the exploratory process that describes the final model from each run (Table 4); additionally, only the full exploratory process results from the best fitting run (S2) are given in see Supplementary Materials 1 (SM1) and discussed. For exploratory step 1 (run S2), the model with an age-aggregation of 7+ (δ + q s,a = 0 for ages 8+) had the lowest AIC and this was selected as the age-aggregation for step 2 (see footnote 2 for details and SM1 Table 1). Overall, the BIC for the fall model fits ranged between approximately 9970 and 9890, 9940 and 9860 for the spring survey and 9970 and 9900 for the Spanish survey, indicating the grouping of the Spanish survey coefficient of variations (CVs) provided the least improvement in model fit (SM1 Tables 2–5). This is not surprising since the data for the Spanish survey do not cover the entire 3LNO region and are not as informative as the fall and spring surveys (see, e.g. Wheeland et al. 2018 for more details). Rechecking the q age-aggregation in Step 3 confirmed that the age-aggregation of 7+ provided the lowest AIC and BIC with the new survey CV formulations (SM1 Table 6). The continuation ratio logit (crl) age exploratory runs in Step 4 had BICs that ranged from approximately 9600 to 9570, and the age aggregation of (5–6)(7–11)(12–14) was selected as the final crl sd age formulation (SM1 Table 7). For Steps 5a and 5b, the BICs ranged from approximately 9560 to 9480 (SM1 Table 8). Rechecking the q’s in Step 6 confirmed that the age-aggregation of 7+ provided the lowest AIC and BIC with the new survey CV and crl sd formulations (SM1 Table 9). The AIC and BIC from Step 1 with a q age-aggregation of 7+ were 9690 and 9922 in comparison to the Step 6 run that were 9194 and 9481 respectively, indicating a substantial improvement in model fit.
Table 4
In all four exploratory model scenarios, q7+ was the best formulation for the survey catchabilities (q; Table 4). Overall, the survey CV formulations were similar for all four model formulations. For example, for the fall survey, models S1–S3 provided identical formulations, with S4 (all AR(1) parameters fixed to zero) providing a better fit with an extra CV parameter for ages (2–4). Both the spring and Spanish CV formulations were similar for all four runs, providing the best fit with separate parameters at the oldest and youngest ages. In all formulations, the best fit for the crl sd parameters had a separate variance parameter from 1990–1999, with various formulations for the age groupings. For example, S1 provided the best fit with separate sd parameters for ages 5–7,14, and pooled for ages (8–13), whereas S4 pooled the sd parameters for ages (5–11) and (12–14). Overall, S2 had the lowest BIC, and had the best residual fits for both the surveys and the crls (see Supplementary Materials 2), and we selected this model as the best fitting model. For the final exploratory step (i.e., one run with all ϕ F parameters freely estimated and all ϕ C fixed and one run with all AR(1) parameters freely estimated), the lowest BIC was for the model with all but the crl AR(1) parameters freely estimated (SSM; Table 5), and this was selected as the final state space model.
Table 5
The SSM fit the data well with no patterns in the survey or continuation ratio logit residual plots (see Supplementary Materials 3). In 2017, recruitment, abundance and spawning stock biomass (SSB) were estimated near the lowest historical levels (Fig. 1). The model predicted landings were estimated within the upper and lower bounds, with the predicted landings closest to the upper bound in the early 80s, and again in 2010 (Fig. 2) and closest to the lower bound in the early 1990s. At ages 1–4, the catchability pattern (Fig. 3) for the fall and spring surveys was lower for the Engels than the Campelen trawl. The differences were most pronounced for ages three and four, with the catchability estimates for the Campelen trawl almost twice as large as for the Engels trawl. For ages 1–5, the process errors (Fig. 4) were close to zero until the mid-nineties. Overall, there were no noticeable trends in the process errors at the older ages. Mohn’s rho for the full retrospective run (Fig. 5) was 0.30 for abundance and -0.19 for recruitment. In comparison to the most recent stock assessment model for Grand Bank American plaice (which we refer to as the VPA), the SSM had a lower Mohn’s rho for SSB at 0.43 compared to 0.69 for the VPA (Fig. 6). Mohn’s rho for aveF for the SSM was almost half the VPA Mohn’s rho, at -0.27 for the SSM and -0.45 for the VPA.
Fig. 1
The overall trends in SSB and aveF were similar for the SSM and the VPA (Fig. 7). Noticeable differences included the SSM predictions of historical SSB (i.e. years 1960–1972) that were larger (but with high uncertainty) than the historical SSB predictions from the VPA. The VPA model also predicted a higher average fishing mortality rate in the early 1990s, at approximately 1.1, with the SSM prediction at approximately 0.80 for the same period.
Fig. 2
The self-simulation study lower 2.5% and upper 97.5% intervals for both SSB and aveF covered zero until the mid-1990s,(Fig. 8), indicating that the simulated samples produced estimates that were similar to the SSM estimates in those years. In the earliest years (1960–1972), the median of relative differences for aveF was mostly positive, with the converse for SSB. After 1990, there was a consistent positive bias in aveF and a negative bias in SSB, except in the final years, where aveF was underestimated and SSB overestimated. The boxplots of parameter estimates (Fig. 9) showed that the largest range were for estimated μ F 5_Pre1995. TMB has an option (see Thorson and Kristensen, 2016) to reduce bias in nonlinear random effects models, and we implemented this method in a self-simulation run as a potential fix to the bias in our self-simulation study (see M4; Table 5). The bias across the entire time series for both SSB and aveF was much larger with the bias-correction turned on (see Supplementary Materials 4) than without. The jittered-start test did not converge for 5% of the simulations, with 100% of the converged models producing negative log-likelihoods that were identical to the original formulation.
Fig. 3
The minimum negative log-likelihood from the M profile likelihood plot was 4472, with an associated Δ M of 0.30 (Fig. 10). For this model fit, the average fishing mortality rate in 2017 was estimated at 0.01 with SSB in 2017 at 100.83 hundred thousand tons. Results from the sensitivity tests (Table 5) showed that the SSM had a lower BIC than the runs that halved the catch bounds (M2) and “fixed” the landings (M3). This is expected because more narrow catch bounds restrict the flexibility of the model. Mohn’s rho for both M1 and M2 for aveF were slightly larger than the Mohn’s rho from the SSM at -0.29 (Fig. 11). Similarly, Mohn’s rho for M1 and M2 for SSB were slightly larger than for the SSM at 0.39.
Discussion
Overall, our state-space model (SSM) that accounted for uncertainties in the landings data and allowed for process errors fit the data well, with no obvious patterns in the survey and continuation ratio logit residual plots (see Supplementary Materials 3). The retrospective patterns were reduced for spawning stock biomass (SSB) and greatly reduced for average fishing mortality for ages 9–14 (aveF) compared to the most recent stock assessment model (VPA).
The M profile plot provided the best fit when M was increased by 0.30, suggesting that the values we used for M’s may be too low. Previous research found evidence that M’s during 1989 to 1996 (Morgan and Brodie, 2001) had increased to 0.53 and the current VPA model and our SSM include this increase. However, since the closure of the commercial fishery, estimates of total mortality rates have remained high for some periods (e.g. Fig. 7 for years 2000–2006), and this may suggest that M is higher than 0.20 in recent years. This is supported by preliminary work that suggests that M has increased since the mid-1990s (COSEWIC, 2009; Morgan et al., 2011). The lack of recovery of the stock has largely been attributed to overfishing, however the mis-specification of M not only in the SSM but in historical assessment models could be over-estimating the relative impact of F. Thus, although a thorough study of M is beyond the scope of this paper, research that improves our understanding of M for this species should be of high priority as we may be fixing M within the model to be lower than is reasonable and subsequently over-stating the contribution of fishing mortality to the lack of recovery of the stock.
Fig. 4
Mohn’s rho from the SSM retrospective analyses for both aveF and SSB were closer to zero than Mohn’s rho from the VPA retrospective analysis, which is a key improvement compared to the current assessment model. Including process error in the population dynamics model helped account for underlying time-varying population processes (e.g. M) that were not accounted for in the VPA, thereby reducing retrospective patterns. There is still evidence of slight retrospective patterns, and this may be caused by underlying spatial or time-varying processes that are mis-specified in the observation model since process errors can only account for misspecifications in the process equations.
Fig. 5
The estimate for survey catchabilityq is defined as the value required to scale swept-area abundance to the population abundance (see e.g. Dickson, 1993; Fraser et al., 2007). An estimate of q less than one implies that fewer fish are caught than occupied the area of the trawl, and a value greater than one implies that more fish are caught than occupied the area. Bryan et al. (2014) found evidence of herding behavior in over 90% of observed flatfish in the presence of survey trawls and this herding underestimates the width used in area swept calculations and can result in q estimates that are greater than one. Therefore, larger q estimates are not unrealistic for American plaice; however, the q estimates from the SSM are very large, with the maximum at 6.7. The maximum q estimate from the SSM is however much smaller than the maximum q estimated from the VPA at 13.6 (Table 26, Wheeland et al. 2018). Additional research is required to better understand why the stock assessment model estimates are so high.
Fig. 6
A difference to note between the SSM and the VPA is that the SSM assumes that the survey indices have a normal distribution with a constant coefficient of variation (CV) whereas the VPA assumes that the log of the survey indices have a lognormal distribution. The lognormal distribution does not allow for zeros in the survey data; however, this assumption may not be appropriate when there are many zeros in the data or when zeros are “true” zeros (i.e.no fish available to be caught). The assumption of normality with a constant CV avoids the problem of dropping zeros altogether. However, the normal distribution assumption supports negative indices which are infeasible. A solution to this problem is to use a truncated normal distribution in place of the normal distribution (e.g. Albertsen et al., 2016). However, a normal distribution with constant CV is virtually identical to a truncated normal distribution when the CV is small. Consider two random variables (e.g.Xand Y) that both have mean μ and a constant coefficient of variation, τ = σ / μ. If X~N(μ, σ = τμ) and Y~TN(μ, σ = τμ; Y > 0) has a truncated normal distribution then their density functions differ by a multiplicative constant that only depends on τ and does not depend on μ. The constant is ∫ 0 ∞ φ(z − 1 _ τ ) dz where φ(∙) is the density function for Z~N(0,1). The constant is close to 1 for τ < 0.5. Hence, for our model, using the truncated normal distribution instead of the normal distribution will only affect estimation through differences in the weighting of survey indices with differentτ’s, especially when τ ≫ 0.5. For our SSM we only have large τ’s for the Spanish survey and ages 1–2 for the Canadian surveys, thus in our case there should be little difference in model fit for the truncated normal vs the normal. However, although the approaches are theoretically similar, future research is needed to compare the performance of the three methods.
Fig. 7
Fitting the age composition and landings data separately is in line with the integrated model philosophy, but our treatment of stock and catch weights is not. Ideally, each source of data should enter independently into the likelihood equation; however, the stock and catch weights at age data for American plaice are collected in complex length-stratified sampling designs and how to model these likelihoods is difficult and beyond the scope of this paper. In the future, state-space stock assessment models will ideally fit to the raw data (e.g., maturity at age, weights at age) and this will require complex stock assessment models that can account for the spatial nature of the stock assessment data.
Fig. 8
The self-simulation study lower 2.5% and upper 97.5% did not cover zero for years 2006–2010 and again in 2013–2015. This bias was also present in models O1 (fixing all crl and F AR(1) parameters) and O2 (freely estimating all AR(1) parameters; (see Supplementary Materials 4). In a self-test simulation the model is specified exactly so stock size estimation bias cannot be the result of model misspecification, but rather it must be related to estimation bias and possibly related to nonlinear modelling of random effects. Our self-simulation run that implemented the TMB bias correction option had larger bias than the SSM self-simulation run without (see Supplementary Materials 4), which provides evidence that the bias is related to estimation bias. Also, preliminary research that fit the SSM with an increase in M (both across the entire time series, and another run increasing M only in the later years) did not produce the self-simulation bias in SSB and aveF in these later years (see Supplementary Materials 4). Hence, it seems that the bias is related to the particular settings of the model, and perhaps the magnitude of variance parameter estimates, and this requires additional research to better understand this type of bias.
Fig. 9
Although M profile plots are useful in providing a general picture of the role of the M assumption, it is also useful to examine which data sources are more informative about M, and Lee et al. (2011) suggested that informative length or age composition data is needed to reliably estimate M. Data-specific M profiles are commonly produced by more traditional stock assessment models without random effects and process error (e.g.SS3; Methot and Wetzel, 2013) but in a state-space stock assessment model it is not straight-forward how to do this because the integrated log-likelihood cannot be split into a sum of log-likelihoods due to various data sources and other model assumptions. Further development of diagnostics designed to detect M misspecification (e.g.Cadigan and Farrell, 2002) also seems useful.
Fig. 10
While overall trends in stock trajectory are similar, our new SSM is an improvement to the current stock assessment model that is used to inform the management of American plaice on the Grand Bank of Newfoundland as it allows for errors in the landings data and reduces the retrospective patterns. Additionally, the thoroughness of our model selection process has the potential to increase the confidence in the selected final model and thereby in the assessment output that is being provided to fisheries managers. Our results also suggest that the current values used for natural mortality rates may be too low as our diagnostic model fitting found the best model fit when M was increased by 0.30. This is an important note not only for American plaice, but for all stocks that are managed under the assumption of a fixed M. We suggest that M profile plots (and/or alternative diagnostics) should be routinely provided to facilitate a better understanding of model behavior for various assumptions about M. This can provide motivation for research into more realistic values of M for future stock assessment models. Overall, this model is a valuable first step in improving our understanding of the stock of American plaice on the Grand Bank of Newfoundland as the flexibility of state-space models are an ideal foundation to build more realistic models.
Fig. 11
Acknowledgements
Research funding was provided by the Ocean Frontier Institute, through an award from the Canada First Research Excellence Fund. Research funding to NC was also provided by the Ocean Choice International Industry Research Chair program at the Marine Institute of Memorial University of Newfoundland. Funding to AP was also provided by a Natural Sciences and Engineering Research Council of Canada Master’s Graduate Scholarship. Many thanks are also extended to Dr. Anders Nielsen, Danish Technical University, for advice on more computationally efficient ways to implement our model in TMB and to the associate editor and two reviewers for their comments and suggestions that greatly improved the final version of this paper.
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