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Michel De Lara, Luc Doyen, Thérèse Guilbaud, Marie-Joëlle Rochet, Is a management framework based on spawning-stock biomass indicators sustainable? A viability approach, ICES Journal of Marine Science, Volume 64, Issue 4, May 2007, Pages 761–767, https://doi.org/10.1093/icesjms/fsm024
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Abstract
Fisheries management agencies have to drive resources on sustainable paths, i.e. within defined boundaries for an indefinite time. The viable-control approach is proposed as a relevant method to deal with sustainability. We analyse the ICES precautionary approach (PA) by means of the notion of viability domain, and provide a mathematical test for sustainability. It is found that the PA based on spawning-stock biomass (SSB) and fishing mortality (F) indicators is sustainable only when recruits make a significant contribution to SSB. In this case, advice based upon SSB, with an appropriate reference point, is sufficient to ensure sustainability. In all other cases, SSB is not a sufficient metric of stock productivity and must be complemented with other management indicators to ensure sustainability. The approach is illustrated with numerical applications to the northern hake and Bay of Biscay anchovy.De Lara, M., Doyen, L., Guilbaud, Th., and Rochet, M-J. 2007. Is a management framework based on spawning-stock biomass indicators sustainable? A viability approach. – ICES Journal of Marine Science, 64: 761–767: 000–000.
Introduction
Sustainability is a major goal of international agreements and guidelines to fisheries management (FAO, 1999; ICES, 2004). However, the meaning and operational content of sustainability is not always well defined. We define sustainability as the ability to maintain a system within the limits of given objectives for an indefinite time.
Sustainability of management framework based on spawning-stock biomass
Indicators and their associated reference points are key elements of current management advice, as well as of the developing ecosystem approach. One or several indicators are used to monitor the progress towards management objectives, be they implicit or explicit. Reference points are selected as benchmarks for the indicator values (Deriso et al., 1998; FAO, 1999; ICES, 2004). In the ICES precautionary approach (PA), the objectives are to maintain spawning-stock biomass (SSB) above a limit reference point Blim, while keeping fishing mortality (F) below a limit reference point Flim (ICES, 2004).
We claim that the indicators in the PA play a confusing double role of implicit sustainability objectives and explicit management tools. The issues at stake are the following. Can the objectives defined by SSB and F be achieved by operational advice based only on SSB and F being used as indicators? Assuming the management would follow the advice and be complied with, would it be sufficient to keep an indicator above a reference point to be able to keep it there again after subsequent time-steps? The answer is far from being obvious, because exploited stocks are not at equilibrium and their dynamics bear a shared inertia.
Optimum-control theory has been extensively used to define fisheries management strategies (Hilborn and Walters, 1992; Quinn and Deriso, 1999). Although it offers a dynamic perspective, undesirable outcomes of optimality approaches undermine its applicability in a sustainability perspective. First, it could be optimal to exhaust the resource. Second, optimum solutions depend largely on the selected discount rate, which measures relative preference for future payoffs with respect to present ones. Moreover, optimum control is not easy to apply when multiple objectives are pursued.
The viability approach put forward here does not strive to determine optimum paths for the co-dynamics of resources and exploitation, but paths belonging to acceptable corridors. These corridors are defined by the management objectives, and sustainability is then defined as the ability to maintain the system within these corridors for an indefinite time. The viable-control approach (Aubin, 1991), or weak-invariance approach (Clarke et al., 1995), enables us to define the corridor borders formally, and allows us to provide advice for decision-making, given a set of objectives, by computing the conditions that allow these objectives to be fulfilled at any time, in the present and in the future. This approach has been applied to renewable-resource management (Béné et al., 2001; Doyen and Béné, 2003; Eisenack et al., 2006; Rapaport et al., 2006), and has been suggested to be useful potentially in integrating ecosystem considerations (Cury et al., 2005). When system dimension increases and/or relationships become non-linear, technical and numerical difficulties in applying viability concepts generally arise. However, in a companion paper (De Lara et al., 2006), we show how viability tools allow us to take advantage of some monotonicity properties of age-structured population models.
Here, we use the viable-control approach to make the relationships between management objectives, the PA, and the stock dynamics explicit. We show how the age-structured dynamics can be taken into account to test whether SSB and F are appropriate indicators for keeping SSB above a reference point. First, the age-structured population dynamics model is presented, together with viability tools. Then, sustainability of the PA is examined. The approach is illustrated with applications to the northern hake and Bay of Biscay anchovy.
Material and methods
Age-structured stock model



Indicators and reference points
Two indicators are used in the PA, with associated limit reference points. Let us stress here that using limit reference points implies defining a boundary between unacceptable and acceptable states, whereas desirable states would rather be defined by target reference points. The first indicator, denoted by SSB in Equation (3), is associated with the reference point Blim > 0. For management advice, an additional precautionary reference point Bpa > Blim is used, intended to incorporate uncertainty about stock state.

The associated limit reference point is Flim and the PA reference point is Fpa < Flim. Acceptable controls λ, according to this reference point, are those for which F(λ) ≤ Flim, because higher F rates might drive SSB below its limit reference point.
Acceptable configurations
To define sustainability, we now assume that the decision-maker can describe “acceptable configurations of the system”, i.e. acceptable couples (N, λ) of states and controls, which form a set 𝔻 ⊂ ℝA+ × ℝ+, the acceptable set. Let us insist upon the fact that 𝔻 includes both system states and controls. In practice, the set 𝔻 may capture ecological, economic, and/or sociological requirements.

Viability domains and viable controls

In other words, if one starts from a stock in 𝕍, there exists an appropriate fishing mortality multiplier such that the system is in an acceptable configuration and the next time-step state is also in 𝕍. For example, acceptable equilibria ((N̄, λ̄) ∈ 𝔻 and g(N̄, λ̄) = N̄) are viability domains.

Interpreting PA in the light of viability


We shall say that the PA is sustainable if the PA state set 𝕍lim given by Equation (8) is a viability domain for dynamics g in the acceptable set 𝔻lim given by (5).
Whenever the PA is sustainable, the set (7) of viable controls Λ𝕍lim(N) is not empty. This implies the existence of a viable fishing mortality multiplier λ ∈ Λ𝕍lim(N) that allows the SSB of the population to remain above Blim at any time. When 𝕍lim is not a viability domain for dynamics g in the acceptable set 𝔻lim, maintaining the SSB above Blim from year to year will not be sufficient to ensure the existence of controls ensuring status quo. For example, in a stock with high abundance in the oldest age class and low abundances in the other age classes, SSB would be above Blim but would be at high risk of falling below Blim the subsequent year, whatever the fishing mortality, if recruitment is low.
Results

Notice that, when γ1 = 0 (the recruits do not reproduce) condition (9) is never satisfied (because πe−MA < 1) and the PA is not sustainable, whatever the value of Blim. In other words, to keep SSB above Blim for an indefinite time, it is not enough to keep it there from year to year. Other conditions based upon more indicators have to be checked.
We stress that condition (9) involves biological characteristics of the population (Table 1) and the S-R relationship φ, as well as the threshold Blim. However, it is important to note that condition (9) does not depend on the S-R relationship φ between 0 and Blim. It does not depend on Flim either.
Parameter definitions and values for two case studies (ICES, 2005b, c).
| Definition . | Notation . | Anchovy . | Hake . |
|---|---|---|---|
| Maximum age | A | 3 | 8 |
| Mean weight-at-age (kg) | (wa)a | (16, 28, 36) × 10−3 | (0.126, 0.2, 0.319, 0.583, 0.986, 1.366, 1.748, 2.42) |
| Maturity ogive | (γa)a | (1, 1, 1) | (0, 0, 0.23, 0.60, 0.90, 1, 1, 1) |
| Natural mortality | M | 1.2 | 0.2 |
| F-at-age | (Fa)a | (0.4, 0.4, 0.4) | (0, 0, 0.1, 0.25, 0.22, 0.27, 0.42, 0.5, 0.5) |
| Presence of plus group | π | 0 | 1 |
| F precautionary RP | Fpa | 1–1.2 | 0.25 |
| SSB precautionary RP (t) | Bpa | 33 000 | 140 000 |
| F limit RP | Flim | / | 0.35 |
| SSB limit RP (t) | Blim | 21 000 | 100 000 |
| Definition . | Notation . | Anchovy . | Hake . |
|---|---|---|---|
| Maximum age | A | 3 | 8 |
| Mean weight-at-age (kg) | (wa)a | (16, 28, 36) × 10−3 | (0.126, 0.2, 0.319, 0.583, 0.986, 1.366, 1.748, 2.42) |
| Maturity ogive | (γa)a | (1, 1, 1) | (0, 0, 0.23, 0.60, 0.90, 1, 1, 1) |
| Natural mortality | M | 1.2 | 0.2 |
| F-at-age | (Fa)a | (0.4, 0.4, 0.4) | (0, 0, 0.1, 0.25, 0.22, 0.27, 0.42, 0.5, 0.5) |
| Presence of plus group | π | 0 | 1 |
| F precautionary RP | Fpa | 1–1.2 | 0.25 |
| SSB precautionary RP (t) | Bpa | 33 000 | 140 000 |
| F limit RP | Flim | / | 0.35 |
| SSB limit RP (t) | Blim | 21 000 | 100 000 |
RP denotes reference point.
Parameter definitions and values for two case studies (ICES, 2005b, c).
| Definition . | Notation . | Anchovy . | Hake . |
|---|---|---|---|
| Maximum age | A | 3 | 8 |
| Mean weight-at-age (kg) | (wa)a | (16, 28, 36) × 10−3 | (0.126, 0.2, 0.319, 0.583, 0.986, 1.366, 1.748, 2.42) |
| Maturity ogive | (γa)a | (1, 1, 1) | (0, 0, 0.23, 0.60, 0.90, 1, 1, 1) |
| Natural mortality | M | 1.2 | 0.2 |
| F-at-age | (Fa)a | (0.4, 0.4, 0.4) | (0, 0, 0.1, 0.25, 0.22, 0.27, 0.42, 0.5, 0.5) |
| Presence of plus group | π | 0 | 1 |
| F precautionary RP | Fpa | 1–1.2 | 0.25 |
| SSB precautionary RP (t) | Bpa | 33 000 | 140 000 |
| F limit RP | Flim | / | 0.35 |
| SSB limit RP (t) | Blim | 21 000 | 100 000 |
| Definition . | Notation . | Anchovy . | Hake . |
|---|---|---|---|
| Maximum age | A | 3 | 8 |
| Mean weight-at-age (kg) | (wa)a | (16, 28, 36) × 10−3 | (0.126, 0.2, 0.319, 0.583, 0.986, 1.366, 1.748, 2.42) |
| Maturity ogive | (γa)a | (1, 1, 1) | (0, 0, 0.23, 0.60, 0.90, 1, 1, 1) |
| Natural mortality | M | 1.2 | 0.2 |
| F-at-age | (Fa)a | (0.4, 0.4, 0.4) | (0, 0, 0.1, 0.25, 0.22, 0.27, 0.42, 0.5, 0.5) |
| Presence of plus group | π | 0 | 1 |
| F precautionary RP | Fpa | 1–1.2 | 0.25 |
| SSB precautionary RP (t) | Bpa | 33 000 | 140 000 |
| F limit RP | Flim | / | 0.35 |
| SSB limit RP (t) | Blim | 21 000 | 100 000 |
RP denotes reference point.



This means that, in the worst case where the whole population would spawn and die in a single time-step, the resulting recruits would be able to restore the spawning biomass to the required level. This does not mean that longer-lived species that do not reproduce as recruits cannot be fished sustainably, but that SSB is not an indicator to monitor them safely and to ensure they will be maintained for more than one year.
Case studies
Our results are applied to two stocks with contrasting life histories (parameters given in Table 1), Bay of Biscay anchovy (Engraulis encrasicolus), a short-lived small pelagic fish, and northern hake (Merluccius merluccius), a longer-lived top predator. Both stocks are currently assessed by ICES as being at risk of reduced reproductive capacity (ICES, 2005b, c). We examine here if this can be ascribed partly to the way management advice has been designed.
Bay of Biscay anchovy
Because the first age class of anchovy accounts for ca. 80% of SSB, the sustainability of the PA will depend on the relationship between the biomass reference point and the stock dynamics, mainly determined by the S-R relationship because there is no plus group. Assuming various S-R relationships, and taking π = 0 (because no plus group is present), we determine whether the PA based on the current value of Blim is sustainable. The answer is given in the final column of Table 2. The second column contains an expression whose value is given in the third column, and has to be compared, according to condition (10), with the threshold in the fourth column.
Bay of Biscay anchovy: sustainability of advice based on the SSB indicator for various S-R relationships.
| S-R relationship . | Condition . | Parameter values . | Threshold . | Sustainable? . |
|---|---|---|---|---|
| Constant (mean) | Rmean≥R | 14 016 × 106 | 1312 × 106 | Yes |
| Constant (geometric mean) | Rgm≥R | 7109 × 106 | 1312 × 106 | Yes |
| Constant (2002) | R2002≥R | 3964 × 106 | 1312 × 106 | Yes |
| Constant (2004) | R2004≥R | 696 × 106 | 1312 × 106 | No |
| Linear | γ1w1r≥1 | 0.84 | 1 | No |
| Ricker | minB≥Blim[⋯]≥Blim | 0 | 21 000 | No |
| S-R relationship . | Condition . | Parameter values . | Threshold . | Sustainable? . |
|---|---|---|---|---|
| Constant (mean) | Rmean≥R | 14 016 × 106 | 1312 × 106 | Yes |
| Constant (geometric mean) | Rgm≥R | 7109 × 106 | 1312 × 106 | Yes |
| Constant (2002) | R2002≥R | 3964 × 106 | 1312 × 106 | Yes |
| Constant (2004) | R2004≥R | 696 × 106 | 1312 × 106 | No |
| Linear | γ1w1r≥1 | 0.84 | 1 | No |
| Ricker | minB≥Blim[⋯]≥Blim | 0 | 21 000 | No |
The answer is given in the final column of the table.
Bay of Biscay anchovy: sustainability of advice based on the SSB indicator for various S-R relationships.
| S-R relationship . | Condition . | Parameter values . | Threshold . | Sustainable? . |
|---|---|---|---|---|
| Constant (mean) | Rmean≥R | 14 016 × 106 | 1312 × 106 | Yes |
| Constant (geometric mean) | Rgm≥R | 7109 × 106 | 1312 × 106 | Yes |
| Constant (2002) | R2002≥R | 3964 × 106 | 1312 × 106 | Yes |
| Constant (2004) | R2004≥R | 696 × 106 | 1312 × 106 | No |
| Linear | γ1w1r≥1 | 0.84 | 1 | No |
| Ricker | minB≥Blim[⋯]≥Blim | 0 | 21 000 | No |
| S-R relationship . | Condition . | Parameter values . | Threshold . | Sustainable? . |
|---|---|---|---|---|
| Constant (mean) | Rmean≥R | 14 016 × 106 | 1312 × 106 | Yes |
| Constant (geometric mean) | Rgm≥R | 7109 × 106 | 1312 × 106 | Yes |
| Constant (2002) | R2002≥R | 3964 × 106 | 1312 × 106 | Yes |
| Constant (2004) | R2004≥R | 696 × 106 | 1312 × 106 | No |
| Linear | γ1w1r≥1 | 0.84 | 1 | No |
| Ricker | minB≥Blim[⋯]≥Blim | 0 | 21 000 | No |
The answer is given in the final column of the table.
Constant recruitment
Assuming a constant R, as is usual in stock projections, the PA is sustainable with Rmean (average over 1987–2004) or even the geometric mean Rgm of low R years (ICES, 2004). Actually, any other R above R ≈ 1 312 × 106 fish defined in (11) will be sustainable. In 2004, however, there was a minimum historical R-value Rmin of 696 × 106 fish, for which the PA is no longer sustainable.
Linear S-R relationship
Assuming a linear S-R relationship φ(B) = rB with r = fbnbsrS0 as e.g. in a Leslie matrix model (ICES, 2005c), where batch fecundity fb = 500 g−1, number of batches per female per year nb = 21, sex ratio sr = 1/2, egg survival to age 1 S0 = 10−5 (Methot, 1989; Motos, 1996), condition (10) becomes γ1w1fbnbsrS0 ≥ 1. Egg survival S0 to age 1 is highly variable. Assuming all other parameters to be known and constant, condition (10) would be satisfied if, and only if, S0 ≥ 1.2 × 10−5, which is not the case with the average value (over 20 y) S0 =10−5 (Methot, 1989). For the given set of parameters, there is no Blim value large enough for the PA to be sustainable, because the asymptotic growth rate of the population is less than 1. With S0 ≥ 1.2 × 10−5, the population growth rate would be ≥1 and the PA advice would be sustainable with any Blim.
Ricker S-R relationship
Assuming a Ricker S-R relationship φ(B) = aBe−bB, where B is measured in tonnes and with parameters a = 0.79 × 106 and b = 1.8 × 10−5 (De Oliveira et al., 2005), the PA is, strictly speaking, not sustainable. This is because the Ricker S-R relationship decreases towards zero when SSB is large: under this assumption, there is a risk in letting the stock grow too large.
This counter-intuitive result stems from the model allowing for unrealistically large numbers. Assuming a very large SSB accumulated in the oldest age class, recruitment would be close to zero, and the lowest possible sum of survivors could decrease below Blim within a single year without any fishing mortality; this is unrealistic, but mathematically possible.
Northern hake
For hake, the PA is never sustainable, because γ1 = 0 (see the discussion above).
Discussion
Because it is based on a single constraining indicator SSB, the PA appears to be sustainable only when the contribution of recruits to the spawning stock is substantial. This is understandable because the PA advice relies upon a short-term perspective, which projects stock dynamics over the next year and does not consider longer-term dynamics. For stocks with a large contribution of recruits to spawning, sustainability of the PA then depends both on stock dynamics, mainly the assumed S-R relationship, and on the biomass reference point, without any need to constrain F below a reference point. The PA for Bay of Biscay anchovy is sustainable for constant recruitment as long as the value used is not too low. We stress that, in accordance with the ICES PA, we make no assumptions about stock dynamics below Blim. However, the minimum observed recruitment Rmin is always provisional. In 2002, Rmin was 3 964 × 106, which was sustainable. In 2004, recruitment decreased to 696 × 106, and the PA was no longer sustainable.
For stocks with a low contribution of recruits to spawning, the SSB-based PA is not sustainable. No SSB reference point would be high enough to prevent stock collapse in future years, because SSB as the sole indicator is not sufficient to manage the stock. This is because, as established by many empirical studies over the past decade (Marshall et al., 1998; Murawski et al., 2001; Marteinsdottir and Begg, 2002), SSB is not a sufficient index of the renewal capacity of a stock. In that case, the PA is not appropriate to ensure sustainable management within the acceptable set 𝔻lim given by (5). The viability approach can be used to examine how additional indicators could be included into the PA to make it sustainable.
We have demonstrated how the viability approach can be used to check the sustainability of a simple objective in relation to a simple single-stock dynamic model. This could be extended to more complex models and/or to different and mutliple objectives. For more complex models, the generalized results of the present study will hold (De Lara et al., 2006) as long as the monotonicity assumption is verified (the more fishing mortality, the less stock at the next time step). For example, mixed fisheries models in which the dynamics of several stocks are linked by the joint pressure exerted by fishing fleets generally satisfy monotonicity properties. The monotonicity assumption will generally not be fulfilled in, for instance, multispecies models including trophic relationships, and adapted methods will have to be developed.
The viability approach provides a convenient tool to reconcile apparently contradictory objectives. It is reasonable for fisheries managers to require not only to preserve resources, but in addition, to be able to allow harvesting at any time. Another reasonable objective could be to provide a minimum yield every year. Our first computations indicate viability domains depending upon SSB among other indicators, partly justifying the PA, but with a more restricted set of options. This may be useful to develop policies aiming at restoring or maintaining stock at the maximum sustainable yield, as required by the Johannesburg summit (UN, 2002). Such a tool will also be useful in the development of an ecosystem approach to fisheries management where, inevitably, contradictory objectives will have to be considered (FAO, 2003; ICES, 2005a).
Acknowledgements
We thank Benoît Mesnil and Verena Trenkel for useful comments on an earlier draft, and Jake Rice, Niels Daan, and Andrew Payne for thoroughly reviewing and editing the manuscript. This work was supported by the French ministère de la Recherche [Action concertée incitative Écologie quantitative (working group MOOREA), 2002] and by the Région Pays de Loire.
References
Appendix
Proof

We assume that Fmin ≤ Flim, so that 𝔻effort,lim is not empty. Fmin corresponds, by (4), to a fishing mortality multiplier λmin≥0, such that F(λmin) = Fmin. The constraint F(λ) ≤ Flim is thus replaced by λ ≤ λmin in the sequel.
We shall coin sustainability of the PA in the minimum-F sense as the property that the set 𝕍lim provides a viability domain associated with dynamics g in the desirable set 𝔻effort,lim. If this viability domain is not empty, F-multipliers larger than the minimum required λmin can keep biomass above Blim at any time, meaning that the fishery should never have to be closed.


We prove (15), which includes condition (9) as a particular case for λmin=0.













