Abstract
Ecological resilience is the capability of an ecosystem to maintain the same structure and function and avoid crossing catastrophic tipping points (i.e. undergoing irreversible regime shifts). While fundamental for management, concrete ways to estimate and interpret resilience in real ecosystems are still lacking. Here, we develop an empirical approach to estimate resilience based on the stochastic cusp model derived from catastrophe theory. The cusp model models tipping points derived from a cusp bifurcation. We extend cusp in order to identify the presence of stable and unstable states in complex natural systems. Our Cusp Resilience Assessment (CUSPRA) has three characteristics: (i) it provides estimates on how likely a system is to cross a tipping point (in the form of a cusp bifurcation) characterized by hysteresis, (ii) it assesses resilience in relation to multiple external drivers and (iii) it produces straightforward results for ecosystem-based management. We validate our approach using simulated data and demonstrate its application using empirical time series of an Atlantic cod population and marine ecosystems in the North Sea and the Mediterranean Sea. We show that Cusp Resilience Assessment is a powerful method to empirically estimate resilience in support of a sustainable management of our constantly adapting ecosystems under global climate change.
Keywords: resilience, regime shifts, tipping points, climate change, stochastic cusp model, ecosystem-based management
1. Introduction
Ecological resilience, i.e. the capability of an ecosystem to maintain the same structure and function under the influence of external drivers, and avoid crossing catastrophic tipping points, is one of the emerging concepts of sustainability [1,2]. While maintaining ecosystems or populations resilient to global cumulative stressors is fundamental for ecosystem health (the condition of a system in which its attributes are in a normal range, i.e. it can provide a range of ecosystem services) [3], we are lacking concrete and simple ways to empirically estimate and interpret ecological resilience in real ecosystems [3–5]. This shortcoming is partly owing to inconsistencies related to the resilience concept (existence of different definitions across disciplines), but especially owing to the inherent complexity of natural systems [6–8]. The lack of solid methodologies to empirically estimate ecological resilience has caused its neglect in ecosystem-based management frameworks. For instance, European maritime policies (such as the European Union’s Marine Strategy Framework Directive (MSFD)) have only partially embraced the concept, even though the understanding of a system’s ecological resilience could facilitate the adoption of more adequate management measures [9–12].
Ecological resilience is embedded within the concept of regime shifts, i.e. nonlinear and abrupt transitions of a system between alternate states that differ in configuration and/or properties [4,13,14]. Indeed, a highly resilient system is able to withstand more pressures, staying clear from tipping points and associated regime shifts [14,15]. As a result, systems with low ecological resilience need to be managed with caution in order to avoid transitions to unwanted configurations [16]. By contrast, if a system is locked within an undesirable state (e.g. an overfished ecosystem), actions to erode its resilience would be needed to facilitate a shift towards a desirable state [4]. Knowledge about past resilience dynamics and regime shifts of ecosystems would help policymakers understand whether a system has undergone abrupt regime changes and identify the relevant external drivers [17–20]. Importantly, reliable empirical ecological resilience estimates are crucial for assessing the ability of a system to recover to previous baselines, often a key objective of ecosystem-based management, or for detecting if the new state is potentially irreversible [21,22].
Resilience-related terminology is still not so strictly defined, rendering its assessment more difficult. For example, in coral reef studies, ‘phase shifts’ are used to describe transitions between ‘alternative stable states’, which may be irreversible, while ‘alternative stable states’ are also used in the context of reversible shifts [23]. Moreover, resilience is a multifaceted concept that is still evolving over time. Besides ecological resilience, that is the focus of this study, resilience may also refer to how fast a system recovers from perturbation (engineering resilience) and whether a system is able to adapt and transform under new pressures (social resilience). Meanwhile, similar concepts like resistance or stability typically refer to a single (current) state, and they are more related to engineering resilience [15]. While measuring ecological and engineering resilience is relatively easy from experiments or theoretical models, the challenge lies in determining resilience from empirical data for large ecological systems that cannot be experimentally manipulated [8,24–26]. A number of methods have been proposed to estimate resilience in aquatic populations, communities and ecosystems [8]. Early warning signals of regime shifts estimate ecological and engineering resilience based on mathematical properties of time series representing the systems [3,4,27]. Other approaches to estimate engineering resilience in ecosystems are based on species interactions and make use of properties of network analysis and food-web modelling [28–30]. Other approaches quantify the ecological resilience of alternate states in probabilistic terms using information from a large number of different systems [31,32] or simulated system states [33], and/or fitting alternative models. Approaches based on model fitting/maximum likelihood can also be used to probe the resilience of complex natural systems [34,35]. A common issue across all these methods is that they generally require large and detailed (empirical or simulated) datasets with high temporal resolution, which are usually unavailable for complex natural systems.
An empirical approach for the detection of regime shifts and the quantification of ecological resilience that makes use of typical ecological monitoring time series is the Integrated Resilience Assessment (IRA) [27,36]. IRA quantifies resilience by identifying two or more multiple stable states of a system, affected by one driver that acts as a system stressor. The system states are identified by testing the fit of multiple models on the response curve of the system to a stressor. If a discontinuous response is identified, the predicted lines of the optimal model represent the attractors and form the basis to estimate the position of the tipping points. Ecological resilience is then estimated based on how far each system state lies from both its attractor and its respective tipping point [27,36–39]. This method has been applied across different marine ecosystems [27,36,38,40,41]. The IRA, has however, the shortcoming that it is a single-driver approach and hence a strong simplification of complex ecological systems that are usually affected by multiple and possibly interacting drivers [42]. Moreover, the underlying statistical model does not represent potential irreversibility [42]. Models based on the catastrophe theory such as the stochastic cusp model (cusp) can better represent irreversible discontinuous dynamics driven by multiple drivers [8,43–46]. Cusp is a nonlinear modelling approach based on a cubic differential equation that allows to identify tipping points derived from a bifurcation in a system depending on two interactive drivers and to test for reversibility of system states [44,45,47,48]. The cusp model started to be used in the early 1970s in different disciplines (such as economics, ecology and behavioural science) but was soon criticized owing to its deterministic framework and the lack of stochasticity [49,50]. The recent addition of the stochastic framework has revived interest in this model that can describe discontinuous dynamics of a state variable around a bifurcation. Expanding cusp to estimate ecological resilience could be a step forward in developing a reliable resilience assessment from empirical data.
Here, we combine the cusp and concepts from IRA’s resilience estimation to develop a Cusp Resilience Assessment (CUSPRA) that has three characteristics: (i) it provides estimates on how likely a system is to cross a tipping point characterized by hysteresis (i.e. ecological resilience), (ii) it assesses resilience in relation to multiple external drivers and (iii) it produces straightforward results for ecosystem-based management. These three characteristics are fundamental for the development of a method that is both easy to apply on typical empirical datasets and facilitates a better understanding of how systems respond to external drivers. We validate CUSPRA using artificial data and demonstrate its application using empirical time-series data related to an Atlantic cod population and ecosystem dynamics in the North Sea and the Mediterranean Sea. We show that CUSPRA provides an advanced methodology to empirically estimate ecological resilience in support of a sustainable management of constantly changing and adapting ecosystems under global climate change.
2. Material and methods
(a). Building the resilience indicator
We built CUSPRA following a four-step approach: (i) select the variables to use in the model, (ii) fit and evaluate the cusp model, (iii) estimate resilience and (iv) assess the results in relation to the interaction of two drivers (figure 1).
Figure 1.
The four steps of CUSPRA. (i) Selecting the variables: the state variable should be a time series that can represent anything from a single population to an ecosystem. If multivariate time series are available, these need to be reduced to an ecosystem metric using a dimension reduction technique such as Principal Component Analysis (PCA). (ii) Fitting the stochastic cusp model: the model, using a cubic differential equation, represents the dynamics of a system from linear and continuous to nonlinear and discontinuous, depending on the combination of the two drivers. (iii) Estimating resilience (RA): projecting the results of the cusp model in two dimensions, an estimate of resilience can be calculated for every state in time depending on the two drivers. Resilience is calculated based on the vertical distance of a point to linearity and on the horizontal distance of a point to the cusp area (in light blue) or tipping point. . In the cusp area, three equilibria, two stable and one unstable, are possible, in the area below the fold. (iv) Analysing resilience depending on the two interactive drivers: CUSPRA allows to understand how resilience changes over time and to compare the results between case study systems.
(i). Steps 1 and 2: Fitting the stochastic cusp model
The first two steps deliver a cusp model as the basis for the resilience estimation. The cusp represents discontinuous changes in a dynamic system depending on two control drivers (electronic supplementary material, figure S1) [47,51]. The system (i.e. a state variable) is represented by a vector of data, typically a time series, and can be anything from abundance estimates of a population to proxies of ecosystem state(s), depending on the system whose resilience we are interested in analysing. The dynamics of the state variable depending on two interactive drivers are modelled with a cubic differential equation extended with a Wiener’s process to add stochasticity (equation (2.1)) [43,44,46]. The rate of change of the system depends on two parameters or factors, α and β.
| (2.1) |
α and β are the two factors whose interaction create a bifurcation for the state variable. α is the asymmetry factor and controls the state of the system, thus inducing system changes, for instance from regime A to regime B. This factor is usually a linear model of one or multiple external drivers that control the dimension of the state variable such as fishing effort in harvested ecosystem systems [47,52,53] (equation (2.2)). A second bifurcation factor β modifies the relationship between the asymmetry factor and the system state from linear continuous to nonlinear and discontinuous and thus shapes the functional form of system dynamics, i.e. if the system approaches the bifurcation. The bifurcation factor is usually a linear model of one or more external drivers that induce changes in the system, such as temperature, eutrophication or climate indices [47,52–54] (equation (2.2)). Abiotic and biotic drivers and their combination can be used to model the three factors fitted in the stochastic cusp model.
| (2.2) |
where α 0, β 0 and w 0 are the intercepts, and α 1, β 1 and w 1 the slopes of the models. SST stands for Sea Surface Temperature.
The choice of which variable represents the bifurcation and the asymmetry factor can be made in different ways. If there is a deep knowledge of the system, the choice can be made ‘a priori’. For instance, in the case of a harvested stock, it is reasonable to believe that fishing is the driver that has the biggest impact on the stock and thus can lead to a shift of the stock from state A to state B, while temperature might have a more indirect effect on the stock by changing its productivity. Thus, in this case, fishing will be fitted as the asymmetry factor and temperature as the bifurcation factor. In other examples, where there is not such a deep knowledge of the systems or the mechanisms of the state variable might be unknown, a model selection based on the Akaike Information Criterion (AIC) could be performed to understand which combination of variables best describes changes in the state variable. In any case, it should be noted that the stochastic cusp model provides a method to prove and describe how the bifurcation may have occurred but does not provide a mechanistic explanation of the phenomenon.
The solution of the cubic differential equation of the model can either detect the multiple equilibria in the state variable, indicating discontinuous dynamics and a regime shift, or identify that just one equilibrium exists, and thus linear continuous dynamics prevail [44,47,48,53]. The model is generally represented in a horizontal plain determined by the combination of the two drivers (figure 1, steps 2 and 3). The system can move in the plain from areas in which just one equilibrium exists, i.e. linear dynamics, to areas with multiple equilibria, i.e. discontinuous dynamics (i.e. a regime shift, the light blue area) (electronic supplementary material, figure S1). This area is also identified as the area below the fold, where tipping points can occur and resilience is low (electronic supplementary material, figure S1) [44,46]. To detect the presence of discontinuous dynamics, Cardan’s discriminant is calculated (equation (2.3)).
| (2.3) |
If the Cardan discriminant is smaller than or equal to 0, then the state variable follows nonlinear discontinuous dynamics and has multiple equilibria, while if it is higher than 0 the system will follow continuous dynamics [46].
Apart from Cardan’s discriminant, the stochastic cusp model directly fits two alternate models, one linear (equation (2.4)) and one logistic (equation (2.5)) in order to select between different dynamics of the system.
| (2.4) |
where g 0 is the intercept of the model, g 1 and g 2 are the slope coefficients of the two control variables and is the normally distributed random error (mean = 0, variance= σ square).
The logistic model, showing nonlinear but continuous dynamics is fitted as:
| (2.5) |
where Z, α and β are canonical variables of the observed state and control variables defined in equation (2.2) and is the 0 mean random disturbance.
Before proceeding with the resilience estimation, it is necessary to evaluate the model and check that the stochastic cusp model is the better model compared with the alternative linear model, since the definition of ecological resilience includes the presence of alternative stable states and irreversible tipping points. We recommend using four criteria to establish whether the cusp is a good model to describe the data [46,47].
-
—
The pseudo R-squared is higher than 0.3. The pseudo R-squared is calculated as 1 − (error variance/var(z)), where the error variance is defined as the difference between the observed values and the mode of the distribution closest to these values.
-
—
The corrected Akaike Information Criterion (AICc) of the cusp model is lower than the AICc of the linear model (by at least 2 units).
-
—
The percentage of points inside the cusp area needs to be more than 10%.
-
—
The estimate of the state variable parameter needs to be significant.
If these four criteria are met, the stochastic cusp model is superior to the alternative model and is a good simplification of the state variable dynamics; thus, it is possible to proceed with the resilience estimation.
Before proceeding, we tested if the four criteria were able to correctly validate the use of the cusp model. To do this we applied the stochastic cusp model to 100 simulated chaotic, random, periodic and ‘cusp’ time series. The periodic time series were generated with a period of 10 time steps and little noise (standard deviation, s.d. = 0.3), the random time series with a mean = 0 and s.d. = 1. The chaotic time series were generated following a logistic map. We fixed the control parameter (r) at 3.9 in order to explore similar types of a chaotic system. Finally, the α and β used in the models were simulated as α being strongly autocorrelated (AR1 = 0.9) and β being normally distributed. The mean of β varied in five different model scenarios, from −2 (mostly linear) to 2 (mostly discontinuous) with an increment of 1. We ran 10 repetitions of each scenario with a time series of 50 time steps. The state variable for the ‘cusp’ time series was then generated from α and β (electronic supplementary material, figure S2). The simulations can be found at: https://github.com/rfrelat/cuspra/tree/master/inst/scripts/simCUSPRA.R.
(ii). Step 3: estimating resilience, building from the IRA
Ecological resilience is estimated similarly to the IRA, by calculating the distance to the instability area determined by the combination of the two control variables (α, β), and using two components, a vertical and a horizontal component [27]. The resilience of the state variable z is high when the combination of the observed control variables (α, β) that define z are far from the bifurcation area while the resilience is low when α, β are within the bifurcation set. Hence, the resilience of the state variable z, which is appropriately modelled by a cusp and defined by two control variables (α, β) depends only on the values of (α, β) and is independent of the value of z. By definition from equation (2.3), the bifurcation set is defined by equation (2.6):
| (2.6) |
The horizontal component of resilience is the distance of from the bifurcation set or instability area equation (2.7).
| (2.7) |
H is negative when inside the bifurcation set (abs(α)< , low resilience) and positive when outside the bifurcation set (higher resilience).
The vertical component is the distance to linearity, defined by the bifurcation variable , representing how discontinuous the system is (equation (2.8)).
| (2.8) |
V is negative when discontinuous and positive when linear (β < 0).
The resilience (Ri) is then the weighted average between the horizontal and the vertical components. We give double weight to the horizontal component (H) to further stress the importance of for the resilience of the system in comparison to the vertical component (equation (2.9)).
| (2.9) |
Highly negative Ri indicates a highly discontinuous system in the bifurcation set, while highly positive values indicate a linear system far from the bifurcation set. We transformed this resilience value (Ri) using hyperbolic tangent transformation to get an indicator of resilience (RA) between 0 and 1, with 0 reflecting low resilience and 1 high resilience (equation (2.10)).
| (2.10) |
In this way, we obtained an indicator that can be comparable across multiple systems and multiple populations. The resilience estimation is computed for every point of the state variable, depending on the two control variables. Thus, if we fit as a state variable the time series of the biomass of a population, for every point in time, a value of RA will be calculated. A low RA (value close to 0) means that with regard to the fluctuation levels of the stressors, the system is unstable, i.e. large changes in state can happen with little changes in the stressor variables and that the system is close to a tipping point (figure 2). On the contrary, a large RA (close to 1) indicates that the system is mostly linear, and thus if the control variables change the system will change linearly (i.e. the system is far from the tipping point) (figure 2). Being based on the cusp our concept of resilience does not test for resilience per se (as a ‘condition’ of the system independently of the variables that may affect it) but estimates the resilience depending on two external drivers and determines how close a system, which presents a cusp bifurcation, lies to a tipping point.
Figure 2.
The CUSPRA resilience indicator (RA). The two-dimensional representation of the stochastic cusp model; for a–c: on the x-axis, α, the driver controlling the dimension of the state variable; on the y-axis, β, the driver controlling whether the relationship between α and the state variable is linear and continuous or nonlinear and discontinuous. In grey, the instability area is determined by the combination of α and β values where three equilibria are possible. The colours of the areas of the two-dimensional panel, correspond to different resilience estimates (pink = 0 and green = 1). (a) The vertical component of resilience where resilience is estimated as the distance from linearity. (b) The horizontal component of resilience is estimated as the horizontal distance from the cusp area. (c) The CUSPRA resilience indicator is obtained by summing the vertical and horizontal resilience estimates. The resilience is lower inside the instability area. (d) The CUSPRA resilience values and the three-dimensional landscape represent the cusp sudden bifurcation.
(iii). Step 4: testing the indicator
To test whether the indicator provides meaningful results, we created state variables from multiple stochastic cusp models having the α variable being strongly autocorrelated (AR1 = 0.9) and the β variable being normally distributed. The mean of β varied in five different model scenarios, from −2 (mostly linear) to 2 (mostly discontinuous) with an increment of 1. We ran 10 repetitions of each scenario with a time series of 50 time steps.
We tested three hypotheses to validate our resilience metric:
Hypothesis 1 (H1): the resilience decreases with the level of nonlinearity (β).
Hypothesis 2 (H2): a state with low resilience has a higher probability of large changes.
Hypothesis 3 (H3): a state with low resilience is linked to anomalously large variance.
H1 helped us to show how the model works, while H2 and H3 validate that our concept of resilience corresponds to the one described in the literature, where a low resilient system exhibits higher variance and higher probability to change [45,55].
To test these hypotheses, we estimated the CUSPRA resilience on each simulation. For H1, we compared the minimum RA to the set level of nonlinearity (β). We expected that the minimum RA decreases with nonlinearity so it should increase with the mean level of β. For H2, we compared the absolute difference between successive state values with the value of RA. We expected that absolute differences would decrease with higher RA. For H3, we computed the variance within a five-time step window, and we compared it to the level of RA. We expected that the variance is low for high resilience, and that the variance increases when resilience decreases.
(b). Data
To test the newly developed indicator, we used data from four published scientific articles using the stochastic cusp model or the IRA and ranging from populations to community and to trait configurations [37,38,48]. We built an R package (cuspra) and a Shiny App to allow all members of the scientific community to test our resilience indicator with their own data (https://rfrelat.shinyapps.io/CUSPRA/). In all three examples, the drivers tested to assess resilience were fishing and temperature (i.e. Sea Surface Temperature (SST)), derived from different sources. The examples are thus comparable. To test population resilience, we used data from the Atlantic cod (Gadus morhua) stock of the northeast Arctic Sea [48]. We used as a proxy for the state of Atlantic cod in the northeast Arctic, Spawning Stock Biomass (SSB) data deriving from stock assessment. Fishing mortality (F), also estimated from stock assessment, and SST were used as drivers to test resilience. The data ranged from 1946 to 2016 [48] (electronic supplementary material, figure S3).
Community resilience was explored using North Sea and Mediterranean Sea data from previous studies. In this case, to build a ‘community state’, first a multivariate reduction technique (PCA) needed to be applied [37]. CUSPRA, similarly to both IRA and the stochastic cusp model, needs to fit a single vector (a time series) representing the system state to the model. The North Sea community state index was built by performing a PCA to a matrix of data coming from the Continuous Plankton Recorder (CPR) and International Bottom Trawl Survey (IBTS) [53]. SST derived from NOAA ErSST v5 and fishing effort (expressed as hours swept per year) from Couce et al. (2019), were used as drivers to test resilience [56,57]. The data ranged from 1985 to 2019 (electronic supplementary material, figure S4) [53]. In the Mediterranean case, a community state was built using landing data extracted from the database of the Food and Agriculture Organization (FAO) of the United Nations and then reduced using a PCA [37]. As drivers, fishing capacity (i.e. cumulative fleet gross tonnage) estimated for the entire EU Mediterranean fleet (EU fleet capacity/gross tonnage) and SST from the NASA PODAAC were used. The data ranged from 1985 until 2013 (electronic supplementary material, figure S5). Finally, to estimate resilience of the biological traits of the Mediterranean Sea community, we used landing traits data [37]. This dataset was derived by combining the Mediterranean fisheries landing data of the FAO for the years 1985–2015 (https://www.fao.org/fishery/en/collection/gfcm_capture?lang=en) with a matrix including data on 23 complete traits related to the biology, ecology, trophic role, distribution, habitat and behaviour of 205 species (mostly fish, but also molluscs and crustaceans) [58]. The multiplication of the two datasets resulted in a matrix of community-weighted mean trait landings by year in the Mediterranean Sea [37] (electronic supplementary material, figure S6).
All analyses were performed in R (version 4.0.2) using the package ‘cusp’ [47] for the cusp modelling. The implementation of the calculation of the resilience indicator (RA) is documented in an R package available in the github repository (https://github.com/rfrelat/Cuspra) and can be downloaded directly in R by typing: devtools::install_github (‘rfrelat/cuspra’). A Shiny app was created and made available to help scientists calculate the resilience indicator on their time series or run other simulations (https://rfrelat.shinyapps.io/CUSPRA/). The data and codes are additionally stored in Dryad [59] and in Zenodo [60].
3. Results
(a). Building the resilience indicator
We have created a protocol to effectively apply CUSPRA (figure 1). The protocol starts with the definition of the system for which the ecological resilience will be estimated as well as the relevant pressures. The system may be described by a single variable (e.g. biomass representing a fish stock) or multiple variables (e.g. abundance of multiple species representing a community). For the latter, applying a reduction technique such as PCA is needed to summarize the multidimensional system into a single variable, so that the stochastic cusp model can be fitted. The model fit must be evaluated before proceeding to the last step, the resilience estimation. The framework, starting from a time series of a state variable and two drivers, provides an estimate of the resilience of the state variable for each combination of the drivers.
(b). Validation
First, we validated the use of the four criteria to correctly classify a time series exhibiting a catastrophic shift. Our results show that the four criteria together have a high power of correctly rejecting the application of a stochastic cusp model to a time series without a cusp bifurcation dynamic. Indeed, there were almost no false positives (1%) and some false negatives (8%). The false positive mostly involved rejecting cusp simulations when there is a low number of points in the cusp areas. The pseudo-R-squared criterion was best at rejecting the application of the stochastic cusp model to random time series, while the delta AICc was best with chaotic and periodic time series (electronic supplementary material, figure S7).
Then, we validated our CUSPRA method by simulating time series of two drivers, α and β, to derive a state variable from the stochastic cusp model. We assumed the α variable to be strongly autocorrelated (AR1 = 0.9) and the β variable to be normally distributed, to imitate, respectively, an anthropogenic driver such as fishing, and a climate variable such as temperature or productivity. The mean of β varied in five different model scenarios, from −2 (mostly linear) to 2 (mostly discontinuous). We ran 10 repetitions of each scenario with a time series of 50 time steps. With these simulations, we tested three hypotheses to evaluate whether our model was meaningful. First, we wanted to show that resilience decreases with the level of nonlinearity (β). A β of – 2 has high resilience while a β of 2 has a resilience close to 0 indicating that the choice of a meaningful bifurcation variable to estimate resilience in real examples is crucial (figure 3a ). The second and third hypotheses were related to the concept of resilience itself, i.e. a system with low RA has a higher probability of change and is linked to larger variances. These two properties are related to the concept of critical slowing down, a property typical of systems approaching a tipping point [28,61]. Using our simulated data, we confirmed that the amount of change of the state variable between two time points t and t +1 (delta Δ) increases and becomes more variable as RA declines (figure 3b ). Moreover, at a low RA the variance of the state variable (calculated with a 5-year moving window) increased (figure 3c ). These results indicate that the resilience estimated by CUSPRA corresponds to the concept of resilience in ecology [4,46,62,63].
Figure 3.
Simulation results for model evaluation. (a) Distribution of the minimum RA resilience (y-axis) for a simulated time series with different mean values of the β drivers (x-axis). (b) Changes in the state variable depending on its resilience (x-axis). The blue line represents the smoothed relationship between these two variables, showing that at lower RA values the probability of change increases. (c) Variance of the state variable depending on its resilience value RA calculated with a 5-year moving window. The blue line represents the smoothed relationship showing that variance decreases with increasing resilience.
(c). Application to real systems
We used four examples to illustrate the application of our new resilience estimation approach. First, we estimated resilience of a commercially important fish stock (Atlantic cod, Gadus morhua) in the northeast Arctic [48] based on fish stock assessment data (modelled population outputs). We used SSB (the weight of mature fish in the stock) as the predictor for the state variable, while α was predicted by fishing mortality (F), and β by SST (for more details about the modelling see Sguotti et al., 2019, electronic supplementary material, figure S2). The cusp model fitted well and was superior to the alternative linear model (electronic supplementary material, table S1). All four validation criteria were met and thus the cusp model fitted well to the data. The analysis shows that at the beginning of the time series the resilience of the stock was low (figure 4a,b ). During that period the stock biomass was low, fishing mortality on a medium level and temperature low as well. The subsequent increase in fishing pressure pushed the stock towards a resilient and hence stable (albeit undesirable) low biomass state, outside the cusp area (figure 4a,b green, small dots). Decreasing fishing mortalities after 2007 coupled with an increase in temperature eroded the resilience of the biomass (pink dots) and moved the system back into the cusp area, leading to a tipping point from a low towards a high biomass state in ca 2009. A further increase in temperature subsequently increased the resilience of the high biomass state (figure 4a,b ). The northeast Arctic cod provides an example in which a management measure (i.e. reduced fishing pressure) eroded the resilience of the unfavourable low biomass state, and in combination with increasing temperatures moved the stock towards a more favourable stable state, representing a positive transition.
Figure 4.
The CUSPRA application. (a,b) Resilience of northeast Arctic cod spawning stock biomass (SSB) depending on fishing mortality and Sea Surface Temperature (SST). (c,d) Resilience of the North Sea ecosystem depending on fishing effort and SST. (e,f) Resilience of the Mediterranean ecosystem based on traits depending on fishing capacity and SST. a,c,e show the time series of resilience in the different systems. b,d,f show the resilience values in the two-dimensional representation of the cusp model with the blue area corresponding to the cusp area where three equilibria are possible, i.e. two stable and one unstable. The dimension of the dots is proportional to the magnitude of the state variable. The colour of the dots corresponds to the colour of our CUSPRA resilience estimate RA, pink = 0, low resilience, green = 1, high resilience.
Next, we applied CUSPRA to the dynamics of entire communities (North Sea and eastern Mediterranean Sea) represented by multivariate datasets. We used as a state variable the first mode of variability derived from the PCA (PC1). We predicted α with a time series of fishing pressure (see §2) and β with SST. The cusp models of the North Sea fitted well and passed the four criteria (electronic supplementary material, table S1). The analyses revealed very low resilience in the North Sea community at the beginning of the time series (figure 4c,d ) when fishing pressure was high and temperature low, and the community was in a state dominated by cod [53]. With decreasing fishing pressure (mainly in the 2000s) and increasing temperature (mainly in the 2010s) the North Sea community changed from low to high resilience owing to structural changes in terms of species composition [53]. On the contrary, the eastern Mediterranean Sea community model did not pass the four criteria. Indeed, the AICc of the linear model was lower than the AICc of the cusp. Therefore, this community presents another type of dynamic that cannot be modelled with CUSPRA.
Finally, we used CUSPRA to estimate resilience of the trait composition of the fish community of the Mediterranean Sea [38]. PC1 here represents the main mode of variability of the trait space of the fish community and was used to predict the state variable in the cusp model. Again, we used a measure of fishing pressure (EU fleet capacity/gross tonnage) and SST to predict the α and β variables, respectively (electronic supplementary material, figure S5). The cusp model fitted well and met all four criteria (electronic supplementary material, table S1). Similar to the analysis of the eastern Mediterranean fish community, resilience decreased initially with increasing fishing pressure (figure 4e,f ). With the decline of fishing capacity and especially the increase in temperature, the system abruptly shifted to a new state (see also Tsimara et al. 2021) in the late 1990s, being however, of low resilience, i.e. prone to further shifts. The analysis denotes that only a drastic reduction of fishing pressure would be able to drive the system towards a resilient state, and the increase of SST will require more drastic management approaches.
4. Discussion
CUSPRA is a new method to assess the resilience of ecological systems based on empirical data. This method provides an estimate of how close a system is to a tipping point (in the form of a cusp bifurcation) and hence to a shift into a new state or regime. Such dynamics are represented in CUSPRA through the application of the stochastic cusp model [64], a mathematical approach that can detect bifurcation in a system and thus identify tipping points [9,46,48,54]. Moreover, CUSPRA estimates resilience based on the effect of multiple interacting drivers and provides an indicator directly applicable to ecosystem-based management. We validated our approach using simulated data and tested our newly developed resilience indicator using four empirical example datasets comprising three different system types, i.e. a fish population, two fish communities and a community of traits [37,38,48]. Interestingly, by using the same drivers in all case studies, we can understand their varying impacts in the different systems. For instance, the increase in temperature in the North Sea ecosystem, coupled with strong management measures (i.e. decreased fishing pressure) [53,65], has led to a new resilient ecosystem state, while in the Mediterranean Sea (in the community example described by traits) similar changes in temperature but an increasing exploitation caused a new state but with low resilience. In the Mediterranean case, fishing pressure appears to be still excessively high and the system is likely closer to its maximum thermal tolerance [66,67]. Our examples demonstrate that CUSPRA is useful to understand the resilience of a system and how close it is to tipping points. Our new method not only advances empirical studies in resilience science but can also be directly applicable in ecosystem management settings, even beyond the marine environment, since it is easily transferable to a variety of systems, not only ecological systems but also socio-ecological, financial or behavioural systems.
Another characteristic of our approach is that resilience is quantified based on the interaction of multiple stressors and thus it quantifies hysteresis to interactive pressures [46,48]. This is a step forward compared with other methods that estimate resilience without accounting for system drivers, or methods such as the IRA, that estimate resilience depending on only one driver [28,36]. In the Anthropocene, multiple drivers acting in an interacting or cumulative fashion are increasingly likely to impact our resources and ecosystems, so methods that can consider a higher level of complexity are more suitable to model real systems [68,69]. It is possible to fit in the CUSPRA even more than two drivers adding multiple variables to the two factors controlling the system states. These would allow for a multidimensional study of resilience [70]. Finally, the estimation of a resilience indicator ranging from 0 to 1 allows the CUSPRA to be easily translatable into management and to be used for comparisons across multiple systems. The simplicity of the final indicator is appealing for management purposes since it constitutes a straightforward, unitless metric indicating whether the system under management is in a state that is rather stable or prone to change. Moreover, the possibility of comparing and understanding the resilience of different populations, ecosystems or socio-ecological systems to the same stressors can improve our knowledge about resilience and favour a better comprehension of this complex concept. Thus, our new method can translate the multifaceted concept of resilience in an easily comprehensible metric that can be used in many different disciplines providing useful information for management purposes. Examples of how to translate the concept into management can be found in electronic supplementary material, table S2.
Our CUSPRA approach takes the quantitative resilience assessment of complex natural systems based on empirical data a step forward. While our new method better represents resilience based on the effect of two interacting drivers, it also shows some limitations linked with the stochastic cusp model regarding the consideration of autocorrelation in the time series of the variables and concerning model evaluation [47,48]. Several indicators hence need to be evaluated before a cusp model can be assessed to be superior to alternative linear and continuous models [47,48], i.e. before CUSPRA can be used to assess resilience. Performing a simulation, we showed that the four criteria used to evaluate the cusp model successfully manage to discriminate true cusp bifurcation dynamics. In all three out of four case examples, the cusp model was found to provide more reliable fits to the data than alternative models, which indicates that these ecological systems exhibited nonlinear and discontinuous dynamics.
The model also presents opportunities for improvement. At present, our approach is ‘data-driven’, and thus it is difficult to make predictions. Indeed, the method can be used to estimate resilience of a system in hindsight only, while it cannot provide inferences about its future development [48,54]. Nevertheless, inspecting the interactive effects of drivers and the position of the state variable relative to the instability area provides information on the likely development in the near future. Other future developments could be to extend CUSPRA to the possibility of detecting more than two stable states. This limitation resides in the cusp model that is only able to depict two alternative states and hence no multiple consecutive tipping points can be assessed. Other bifurcation models, such as the ‘butterfly’, should be able to detect more than two stable states and thus could also be integrated in CUSPRA [46]. Nevertheless, usually empirical time series are short, and it is reasonable to believe that only two states of the system likely exist in the data time scales. If longer time series are to be fitted to the data, an extensive data analysis before fitting the CUSPRA is necessary. Visualizing the development of the state variable will show if fitting two separate CUSPRA models is necessary [71]. Other types of bifurcation which resemble the cusp (e.g. Hopf, Neimark-Sacker) might arise in natural systems. At present, our model and indicator might have difficulties in discriminating these bifurcations. However, CUSPRA is the first developed indicator that estimates resilience from bifurcations in empirical systems, and therefore, it is already an important step forward in ecology. CUSPRA models very complex phenomena in a simplistic way [9]. While this simplification could be criticized, it is one of the strengths of this approach, as it makes CUSPRA outputs easily translatable into management. Nonetheless, it would be beneficial for a CUSPRA analysis to be supported by additional indicators aiming to better understand the system state.
(a). How could CUSPRA be used in ecosystem-based management settings?
First, knowledge on the type of dynamics that the system has exhibited in the past (linear or discontinuous) is important to understand if a system is vulnerable to regime shifts [10]. Knowing which drivers have caused the discontinuous dynamics, can give an indication on the resilience of the system towards these drivers, and thus how vulnerable the system is to them [5,72]. This is important for management since it can help to establish which drivers need to be managed in a more precautionary approach in order to enhance the resilience of the system and avoid the crossing of a tipping point [73]. Moreover, CUSPRA can determine the levels of the stressors at which the system will switch into a new state, i.e. the position of the tipping point. This is important knowledge for managers since it can help to mitigate stressors in order to avoid their critical levels [5,74]. Finally, the method gives a snapshot of the resilience of the system at present and thus can indicate whether a system will approach a tipping point in the immediate future. This is particularly important information in order to decide whether to adopt precautionary approaches or whether to try to restore the system towards initial conditions [5]. More precisely, if CUSPRA estimates low ecological resilience for a system, then management could apply a precautionary approach in order to avoid the tipping point. Instead, if a system shows high resilience, restoration towards a previous baseline might be impossible and management should be more focused on aiming for a sustainable transformation and maintaining the new status of the system. Potentially, applying CUSPRA using multiple drivers and their combinations could help managers to define a safe operating space of the system and thus favour better management approaches [75,76]. Estimating resilience is fundamental to properly managing natural systems; however, this concept is seldomly included in management owing to methodological limitations [2,3]. By estimating resilience of ecological systems impacted by multiple stressors, CUSPRA allows for a better quantification of resilience and a direct application to management which is urgently needed if we want to manage constantly changing and adapting systems under global climate change [23,77].
Acknowledgements
The work reflects only the author’s/authors’ view; the European Commission and their executive agency are not responsible for any use that may be made of the information the work contains. We acknowledge the ICES Working Group COMEDA (Comparative Ecosystem-based Analyses of Atlantic and Mediterranean marine systems) under which this study was started and developed. We would like to thank Prof. Christian Moellmann for his precious advices and his brilliant suggestions while developing the study.
Contributor Information
Camilla Sguotti, Email: camilla.sguotti@unipd.it.
Paraskevas Vasilakopoulos, Email: paris.vasilakopoulos@ec.europa.eu.
Evangelos Tzanatos, Email: tzanatos@upatras.gr.
Romain Frelat, Email: rom.frelat@gmail.com.
Ethics
This work did not require ethical approval from a human subject or animal welfare committee.
Data accessibility
The data are stored in Dryad [59]. The codes are available in Zenodo [60]. The package to perform the model can be downloaded directly in R by typing: devtools::install_github (rfrelat/cuspra). A Shiny App was also developed to allow other researchers or stakeholders to easily try the method with their data or simulated data (https://rfrelat.shinyapps.io/CUSPRA).
Supplementary material is available online [78].
Declaration of AI use
We have not used AI-assisted technologies in creating this article.
Authors’ contributions
C.S.: conceptualization, formal analysis, investigation, methodology, resources, validation, visualization, writing—original draft, writing—review and editing; P.V.: investigation, methodology, validation, writing—review and editing; E.T.: investigation, methodology, validation, writing—review and editing; R.F.: conceptualization, formal analysis, investigation, methodology, validation, visualization, writing—review and editing.
All authors gave final approval for publication and agreed to be held accountable for the work performed therein.
Conflict of interest declaration
We declare we have no competing interests.
Funding
C.S. was funded by the EU HORIZON RESET (Resilience Estimation to SET management goals in marine ecosystems) Project (101065994) under the HORIZON-MSCA-2021-PF and by the BMBF-funded project SeaUseTip, Spatio-temporal analysis of tipping points in the socio-ecological system of the North Sea (funding code: 01LC1825A-C). This work is also a contribution to the EU H2020 COMFORT project that received funding from the European Union’s Horizon 2020 research and innovation program under grant agreement number 820989 (project COMFORT, Our common future ocean in the Earth system–quantifying coupled cycles of carbon, oxygen and nutrients for determining and achieving safe operating spaces with respect to tipping points).
References
- 1. Darling ES, Côté IM. 2018. Seeking resilience in marine ecosystems. Science 359 , 986–987. ( 10.1126/science.aas9852) [DOI] [PubMed] [Google Scholar]
- 2. Biggs R, et al. 2012. Toward principles for enhancing the resilience of ecosystem services. Annu. Rev. Environ. Resour. 37 , 421–448. ( 10.1146/annurev-environ-051211-123836) [DOI] [Google Scholar]
- 3. Lu Y, Wang R, Zhang Y, Su H, Wang P, Jenkins A, Ferrier RC, Bailey M, Squire G. 2015. Ecosystem health towards sustainability. Ecosyst. Health Sustain. 1 , 1–15. ( 10.1890/EHS14-0013.1) [DOI] [Google Scholar]
- 4. Scheffer M, Carpenter SR, Dakos V, Nes E. 2015. Generic indicators of ecological resilience: inferring the change of a critical tranistion. Annu. Rev. Ecol. Evol. Syst. 46 , 145–167. ( 10.1146/annurev-ecolsys-112414-054242) [DOI] [Google Scholar]
- 5. Sguotti C, Färber L, Romagnoni G. 2022. Regime shifts in coastal marine ecosystems: theory, methods and management perspectives. Reference module in earth systems and environmental sciences. Amsterdam: Elsevier BV. ( 10.1016/B978-0-323-90798-9.00004-4) [DOI] [Google Scholar]
- 6. Thrush SF, Hewitt JE, Dayton PK, Coco G, Lohrer AM, Norkko A, Norkko J, Chiantore M. 2009. Forecasting the limits of resilience: integrating empirical research with theory. Proc. Royal Soc. B Biol. Sci. 276 , 3209–3217. ( 10.1098/rspb.2009.0661) [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7. Johnson AF, Lidström S. 2018. The balance between concepts and complexity in ecology. Nat. Ecol. Evol. 2 , 585–587. ( 10.1038/s41559-018-0507-5) [DOI] [PubMed] [Google Scholar]
- 8. Donohue I, et al. 2016. Navigating the complexity of ecological stability. Ecol. Lett. 19 , 1172–1185. ( 10.1111/ele.12648) [DOI] [PubMed] [Google Scholar]
- 9. Dakos V, Kéfi S. 2022. Ecological resilience: what to measure and how. Environ. Res. Lett. 17 , 043003. ( 10.1088/1748-9326/ac5767) [DOI] [Google Scholar]
- 10. Selkoe KA, et al. 2015. Principles for managing marine ecosystems prone to tipping points. Ecosyst. Health Sustain. 1 , 1–18. ( 10.1890/EHS14-0024.1) [DOI] [Google Scholar]
- 11. Hughes TP, Carpenter S, Rockström J, Scheffer M, Walker B. 2013. Multiscale regime shifts and planetary boundaries. Trends Ecol. Evol. 28 , 389–395. ( 10.1016/j.tree.2013.05.019) [DOI] [PubMed] [Google Scholar]
- 12. Levin SA, Lubchenco J. R. 2008. Robustness, and marine ecosystem-based management. BioScience 58 , 27–32. ( 10.1641/B580107) [DOI] [Google Scholar]
- 13. Mumby PJ, Chollett I, Bozec YM, Wolff NH. 2014. Ecological resilience, robustness and vulnerability: how do these concepts benefit ecosystem management? Curr. Opin. Environ. Sustain. 7 , 22–27. ( 10.1016/j.cosust.2013.11.021) [DOI] [Google Scholar]
- 14. Scheffer M, Carpenter S, Foley JA, Folke C, Walker B. 2001. Catastrophic shifts in ecosystems. Nature 413 , 591–596. ( 10.1038/35098000) [DOI] [PubMed] [Google Scholar]
- 15. Beisner BE, Haydon DT, Cuddington K. 2003. Alternative stable states in ecology. Front. Ecol. Environ. 1 , 376–382. ( 10.1890/1540-9295(2003)001[0376:ASSIE]2.0.CO;2) [DOI] [Google Scholar]
- 16. Walker B, Holling CS, Carpenter SR, Kinzig A. 2004. Resilience, adaptability and transformability in social-ecological systems. Ecol. Soc 9(2) , 5. ( 10.5751/ES-00650-090205) [DOI] [Google Scholar]
- 17. Sguotti C, Cormon X. RS. 2018. A global challenge for the sustainable use of our marine resources. In YOUMARES 8 – oceans across boundaries: learning from each other pp. 155–166. Springer International Publishing: Cham. ( 10.1007/978-3-319-93284-2) [DOI] [Google Scholar]
- 18. DeYoung B, Barange M, Beaugrand G, Harris R, Perry RI, Scheffer M, Werner F. 2008. Regime shifts in marine ecosystems: detection, prediction and management. Trends Ecol. Evol. 23 , 402–409. ( 10.1016/j.tree.2008.03.008) [DOI] [PubMed] [Google Scholar]
- 19. Litzow MA, Mueter FJ, Hobday AJ. 2014. Reassessing regime shifts in the North Pacific: incremental climate change and commercial fishing are necessary for explaining decadal-scale biological variability. Glob. Chang. Biol. 20 , 38–50. ( 10.1111/gcb.12373) [DOI] [PubMed] [Google Scholar]
- 20. Litzow MA, Hunsicker ME. 2016. Early warning signals, nonlinearity, and signs of hysteresis in real ecosystems. Ecosphere 7(12) , e01614. ( 10.1002/ecs2.1614) [DOI] [Google Scholar]
- 21. Tomczak MT, et al. 2022. Reference state, structure, regime shifts, and regulatory drivers in a coastal sea over the last century: the Central Baltic Sea case. Limnol. Oceanogr. 67 , S266–S284. ( 10.1002/lno.11975) [DOI] [Google Scholar]
- 22. Dakos V, Matthews B, Hendry AP, Levine J, Loeuille N, Norberg J, Nosil P, Scheffer M, De Meester L. 2019. Ecosystem tipping points in an evolving world. Nat. Ecol. Evol. 3 , 355–362. ( 10.1038/s41559-019-0797-2) [DOI] [PubMed] [Google Scholar]
- 23. Ingeman KE, Samhouri JF, Stier AC. 2019. Ocean recoveries for tomorrow’s Earth: hitting a moving target. Science 363 , eaav1004. ( 10.1126/science.aav1004) [DOI] [PubMed] [Google Scholar]
- 24. Fung T, Seymour RM, Johnson CR. 2011. Alternative stable states and phase shifts in coral reefs under anthropogenic stress. Ecology 92 , 967–982. ( 10.1890/10-0378.1) [DOI] [PubMed] [Google Scholar]
- 25. Stelzer JAA, Mesman JP, Adrian R, Ibelings BW. 2021. Early warning signals of regime shifts for aquatic systems: can experiments help to bridge the gap between theory and real-world application? Ecol. Complex. 47 , 100944. ( 10.1016/j.ecocom.2021.100944) [DOI] [Google Scholar]
- 26. Scheffer M, et al. 1979. Anticipating critical transitions. Science 338 , 344–348. ( 10.1126/science.1225244) [DOI] [PubMed] [Google Scholar]
- 27. Dakos V, et al. 2012. Methods for detecting early warnings of critical transitions in time series illustrated using simulated ecological data. PLoS One 7 , e41010. ( 10.1371/journal.pone.0041010) [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28. Scheffer M, et al. 2009. Early-warning signals for critical transitions. Nature 461 , 53–59. ( 10.1038/nature08227) [DOI] [PubMed] [Google Scholar]
- 29. May RM. 1972. Will a large complex system be stable? Nature 238 , 413–414. ( 10.1038/238413a0) [DOI] [PubMed] [Google Scholar]
- 30. Ushio M, Hsieh CH, Masuda R, Deyle ER, Ye H, Chang CW, Sugihara G, Kondoh M. 2018. Fluctuating interaction network and time-varying stability of a natural fish community. Nature 554 , 360–363. ( 10.1038/nature25504) [DOI] [PubMed] [Google Scholar]
- 31. Allesina S, Tang S. 2012. Stability criteria for complex ecosystems. Nature 483 , 205–208. ( 10.1038/nature10832) [DOI] [PubMed] [Google Scholar]
- 32. Hirota M, Holmgren M, Van Nes EH, Scheffer M. 2011. Global resilience of tropical forest and savanna to critical transitions. Science 334 , 232–235. ( 10.1126/science.1210657) [DOI] [PubMed] [Google Scholar]
- 33. Scheffer M, Hirota M, Holmgren M, Van Nes EH, Chapin FS. 2012. Thresholds for boreal biome transitions. Proc. Natl Acad. Sci. USA 109 , 21384–21389. ( 10.1073/pnas.1219844110) [DOI] [PMC free article] [PubMed] [Google Scholar]
- 34. Mumby PJ, Hastings A, Edwards HJ. 2007. Thresholds and the resilience of Caribbean coral reefs. Nature 450 , 98–101. ( 10.1038/nature06252) [DOI] [PubMed] [Google Scholar]
- 35. van Belzen J, et al. 2017. Vegetation recovery in tidal marshes reveals critical slowing down under increased inundation. Nat. Commun. 8 , 15811. ( 10.1038/ncomms15811) [DOI] [PMC free article] [PubMed] [Google Scholar]
- 36. Vasilakopoulos P, Marshall CT. 2015. Resilience and tipping points of an exploited fish population over six decades. Glob. Chang. Biol. 21 , 1834–1847. ( 10.1111/gcb.12845) [DOI] [PubMed] [Google Scholar]
- 37. Vasilakopoulos P, Raitsos DE, Tzanatos E, Maravelias CD. 2017. Resilience and regime shifts in a marine biodiversity hotspot. Sci. Rep. 7 , 13647. ( 10.1038/s41598-017-13852-9) [DOI] [PMC free article] [PubMed] [Google Scholar]
- 38. Tsimara E, Vasilakopoulos P, Koutsidi M, Raitsos DE, Lazaris A, Tzanatos E. 2021. An integrated traits resilience assessment of Mediterranean fisheries landings. J. Anim. Ecol. 90 , 2122–2134. ( 10.1111/1365-2656.13533) [DOI] [PubMed] [Google Scholar]
- 39. Hidalgo M, Vasilakopoulos P, García-Ruiz C, Esteban A, López-López L, García-Gorriz E. 2022. Resilience dynamics and productivity-driven shifts in the marine communities of the Western Mediterranean Sea. J. Anim. Ecol. 91 , 470–483. ( 10.1111/1365-2656.13648) [DOI] [PMC free article] [PubMed] [Google Scholar]
- 40. Ma S, et al. 2021. Critical transitions and ecological resilience of large marine ecosystems in the Northwestern Pacific in response to global warming. Glob. Chang. Biol. 27 , 5310–5328. ( 10.1111/gcb.15815) [DOI] [PubMed] [Google Scholar]
- 41. Polo J, Punzón A, Vasilakopoulos P, Somavilla R, Hidalgo M. 2022. Environmental and anthropogenic driven transitions in the demersal ecosystem of Cantabrian Sea. ICES J. Mar. Sci. 79 , 2017–2031. ( 10.1093/icesjms/fsac125) [DOI] [Google Scholar]
- 42. Damalas D, Sgardeli V, Vasilakopoulos P, Tserpes G, Maravelias C. 2021. Evidence of climate-driven regime shifts in the Aegean Sea’s demersal resources: a study spanning six decades. Ecol. Evol. 11 , 16951–16971. ( 10.1002/ece3.8330) [DOI] [PMC free article] [PubMed] [Google Scholar]
- 43. Fulton EA, Gray R, Sporcic M, Scott R, Hepburn M. 2009. Challenges of crossing scales and drivers in Modelling Marine systems. In 18th world Imacs Congress and Modsim09 International Congress on Modelling and simulation: Interfacing Modelling and simulation with mathematical and computational sciences. ISBN: 978-0-9758400-7-8 (eds Anderssen RS, Braddock RD, Newham LTH), pp. 2108–2114. [Google Scholar]
- 44. Thom R. 1975. Structural stability and morphogenesis. New York: Benjamin/cummings Publishing. [Google Scholar]
- 45. Diks C, Wang J. 2016. Can a stochastic cusp catastrophe model explain housing market crashes? J. Econ. Dyn. Control 69 , 68–88. ( 10.1016/j.jedc.2016.05.008) [DOI] [Google Scholar]
- 46. Petraitis PS, Dudgeon SR. 2016. Cusps and butterflies: multiple stable states in marine systems as catastrophes. Mar. Freshwater Res. 67 , 37–46. ( 10.1071/MF14229) [DOI] [Google Scholar]
- 47. Grasman RPPP, Maas HLJVD, Wagenmakers E. 2009. Fitting the cusp catastophe in R: a cusp package Primer. J. Stat. Softw. 32 , 1–25. ( 10.18637/jss.v032.i08) [DOI] [Google Scholar]
- 48. Sguotti C, Otto SA, Frelat R, Langbehn TJ, Ryberg MP, Lindegren M, Durant JM, Chr Stenseth N, Möllmann C. 2019. Catastrophic dynamics limit Atlantic cod recovery. Proc. R. Soc. B 286 , 20182877. ( 10.1098/rspb.2018.2877) [DOI] [PMC free article] [PubMed] [Google Scholar]
- 49. Petraitis PS, Dudgeon SR. 2015. Variation in recruitment and the establishment of alternative community states. Ecology 96 , 3186–3196. ( 10.1890/14-2107.1) [DOI] [PubMed] [Google Scholar]
- 50. Guckenheimer J. 1977. The catastrophe controversy. Biomathematics 1 , 15–20. [Google Scholar]
- 51. Barkley Rosser Jr J. 2007. The rise and fall of catastrophe theory applications in economics: Was the baby thrown out with the bathwater? J. Econ. Dyn. Control 31 , 3255–3280. ( 10.1016/j.jedc.2006.09.013) [DOI] [Google Scholar]
- 52. Jones DD. 1977. Catastrophe theory applied to ecological systems. Simulation 29 , 1–15. ( 10.1177/003754977702900102) [DOI] [Google Scholar]
- 53. Sguotti C, et al. 2022. Irreversibility of regime shifts in the North Sea. Front. Mar. Sci. 9 , 1830. ( 10.3389/fmars.2022.945204) [DOI] [Google Scholar]
- 54. Möllmann C, Cormon X, Funk S, Otto SA, Schmidt JO, Schwermer H, Sguotti C, Voss R, Quaas M. 2021. Tipping point realized in cod fishery. Sci. Rep. 11 , 1–12. ( 10.1038/s41598-021-93843-z) [DOI] [PMC free article] [PubMed] [Google Scholar]
- 55. Blöcker AM, Sguotti C, Möllmann C. 2023. Discontinuous dynamics in North Sea cod Gadus morhua caused by ecosystem change. Mar. Ecol. Prog. Ser. 713 , 133–149. ( 10.3354/meps14342) [DOI] [Google Scholar]
- 56. Huang B, et al. 2017. Extended reconstructed sea surface temperature, version 5 (ERSSTv5): upgrades, validations, and intercomparisons. J. Clim. 30 , 8179–8205. ( 10.1175/JCLI-D-16-0836.1) [DOI] [Google Scholar]
- 57. Couce E, Schratzberger M, Engelhard G. 2019. Reconstructing three decades of total international trawling effort in the North Sea. Earth Syst. Sci. Data 12 , 373–386. ( 10.5194/essd-2019-90) [DOI] [Google Scholar]
- 58. Koutsidi M, Moukas C, Tzanatos T. 2019. Koutsidi, Moukas, Tzanatos: 23 biological traits of 235 species. See https://figshare.com/articles/dataset/Koutsidi_Moukas_Tzanatos_23_biological_traits_of_235_species/11347406.
- 59. Sguotti C, Vasilakopoulos P, Tzanatos E, Frelat R. 2024. Resilience Assessment in Complex Natural Systems ( 10.5061/dryad.44j0zpcnb) [DOI] [PMC free article] [PubMed]
- 60. Sguotti C, Vasilakopoulos P, Tzanatos E, Frelat R. 2024. Resilience Assessment in Complex Natural Systems ( 10.5281/zenodo.10912017) [DOI] [PMC free article] [PubMed]
- 61. Dakos V, Scheffer M, van Nes EH, Brovkin V, Petoukhov V, Held H. 2008. Slowing down as an early warning signal for abrupt climate change. Proc. Natl Acad. Sci. USA 105 , 14308–14312. ( 10.1073/pnas.0802430105) [DOI] [PMC free article] [PubMed] [Google Scholar]
- 62. Bissell JJ. 2022. Bifurcation, stability, and critical slowing down in a simple mass–spring system. Mech. Res. Commun. 125 , 103967. ( 10.1016/j.mechrescom.2022.103967) [DOI] [Google Scholar]
- 63. Dakos V, Carpenter SR, van Nes EH, Scheffer M. 2015. Resilience indicators: prospects and limitations for early warnings of regime shifts. Phil. Trans. R. Soc. B 370 , 20130263. ( 10.1098/rstb.2013.0263) [DOI] [Google Scholar]
- 64. Thom R. 1977. Structural stability, catastrophe theory and applied mathematics. The John yon Neumann Lecture. SIAM REVIEW 19 . ( 10.1137/1019036) [DOI] [Google Scholar]
- 65. Emeis KC, et al. 2015. The North Sea — a shelf sea in the anthropocene. J. Mar. Syst. 141 , 18–33. ( 10.1016/j.jmarsys.2014.03.012) [DOI] [Google Scholar]
- 66. Cardinale M, Scarcella G, Osio GC, Scarcella GC. 2017. Mediterranean Sea: a failure of the European fisheries management system. Front. Mar. Sci. 4 , 72. ( 10.3389/fmars.2017.00072) [DOI] [Google Scholar]
- 67. Tzanatos E, Raitsos DE, Triantafyllou G, Somarakis S, Tsonis AA. 2014. Indications of a climate effect on Mediterranean fisheries. Clim. Change 122 , 41–54. ( 10.1007/s10584-013-0972-4) [DOI] [Google Scholar]
- 68. Hodgson EE, Halpern BS. 2019. Investigating cumulative effects across ecological scales. Conserv. Biol. 33 , 22–32. ( 10.1111/cobi.13125) [DOI] [PubMed] [Google Scholar]
- 69. Halpern BS, et al. 2008. A global map of human impact on marine ecosystems. Science 319 , 948–952. ( 10.1126/science.1149345) [DOI] [PubMed] [Google Scholar]
- 70. Blöcker AM, Gutte HM, Bender RL, Otto SA, Sguotti C, Möllmann C. 2023. Regime shift dynamics, tipping points and the success of fisheries management. Sci. Rep. 13 , 1–111. ( 10.1038/s41598-022-27104-y) [DOI] [PMC free article] [PubMed] [Google Scholar]
- 71. Sguotti C, Bischoff A, Conversi A, Mazzoldi C, Möllmann C, Barausse A. 2022. Stable landings mask irreversible community reorganizations in an overexploited Mediterranean ecosystem. J. Anim. Ecol. 91 , 2465–2479. ( 10.1111/1365-2656.13831) [DOI] [PubMed] [Google Scholar]
- 72. Rocha JC, Yletyinen J, Biggs R, Blenckner T, Peterson G. 2015. Marine regime shifts: drivers and impacts on ecosystems services. Phil. Trans. R. Soc. B 370 , 20130273. ( 10.1098/rstb.2013.0273) [DOI] [Google Scholar]
- 73. King JR, McFarlane GA, Punt AE. 2015. Shifts in fisheries management: adapting to regime shifts. Phil. Trans. R. Soc. B 370 , 20130277. ( 10.1098/rstb.2013.0277) [DOI] [Google Scholar]
- 74. Samhouri JF, et al. 2017. Defining ecosystem thresholds for human activities and environmental pressures in the California Current. Ecosphere 8 , e01860. ( 10.1002/ecs2.1860) [DOI] [Google Scholar]
- 75. Carpenter SR, et al. 2017. Defining a safe operating space for inland recreational fisheries. Fish Fish 18 , 1150–1160. ( 10.1111/faf.12230) [DOI] [Google Scholar]
- 76. Rockström J, et al. 2009. A safe operating space for humanity. Nature 461 , 472–475. ( 10.1038/461472a) [DOI] [PubMed] [Google Scholar]
- 77. Hughes TP, Linares C, Dakos V, van de Leemput IA, van Nes EH. 2013. Living dangerously on borrowed time during slow, unrecognized regime shifts. Trends Ecol. Evol. 28 , 149–155. ( 10.1016/j.tree.2012.08.022) [DOI] [PubMed] [Google Scholar]
- 78. Sguotti C, Vasilakopoulos P, Tzanatos E, Frelat R. 2024. Supplementary material from: Resilience assessment in complex natural systems. Figshare ( 10.6084/m9.figshare.c.7197878) [DOI] [PMC free article] [PubMed]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Data Availability Statement
The data are stored in Dryad [59]. The codes are available in Zenodo [60]. The package to perform the model can be downloaded directly in R by typing: devtools::install_github (rfrelat/cuspra). A Shiny App was also developed to allow other researchers or stakeholders to easily try the method with their data or simulated data (https://rfrelat.shinyapps.io/CUSPRA).
Supplementary material is available online [78].




