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Using ecosystem modeling for fisheries management Villy Christensen IncoFish WP4 Workshop Cape Town, September 2006 Are ecosystem models useful for fisheries management? 2 “One of those really smart quotes” “We believe the food web modelling approach is hopeless as an aid to formulating management advice; the number of parameters and assumptions required are enormous.” Hilborn and Walters (1992, p. 448) 3 Willie asked the right question... • Why don’t the fish eat them all, dad? 4 5 A key aspect of EwE modeling: • Prey behavior limits predation (foraging arena assumptions) 6 Organisms are not chemicals! Ecological interactions are highly organized Reaction vat model Prey eaten Foraging arena model Prey eaten Predator handling limits rate Prey density Prey behavior limits rate Prey density Big effects from small changes in space/time scale 7 Foraging arena Predator, P aVP Available prey, V Unavailable prey B-V v = behavioral exchange rate (‘vulnerability’); predator-prey specific; 8 based on foraging arena theory (Walters and Juanes, 1993) Time predictions from an ecosystem model of the Georgia Strait, 1950-2000 With mass-action (Lotka-Volterra) interactions only: With foraging arena interactions: 9 A critical parameter: vulnerability 10 Top-down/bottom-up “control” & carrying capacity Predation mortality: effect of vulnerability Predicted predation mortality V= =2 Ecopath baseline 0 Carrying capacity Predator abundance Top-Down High v Bottom-up Low v 11 So how do we get estimates of carrying capacity? • Surveys • Assessments Numbers (x 1000) – Stock reduction analysis Blue whales Fin whales Year Year 12 Christensen, LB, 2006 Evaluation of simulations • Can the model – replicate historic trends? – make plausible extrapolations to novel situations? 13 Fitting to time series: learning from ecosystem history • A proliferation of ecosystem modeling activities has in recent years produced many apparently credible models that fit historical data well and make reasonable policy predictions 14 Ecosystems where EwE models have been tested using historical trend data • • • • • • • • • • • • • E Bering Sea Aleutian Islands W&C GoAlaska E GoAlaska W Vancouver Island Hecate Strait British Columbia Shelf Strait of Georgia NE Pacific CN & ET Pacific NWHI, Hawaii Gulf of California Central Chile • • • • • • • • • • • • Bay of Quinte Oneida Lake Scotian Shelf Chesapeake Bay Tampa Bay S Brazil Bight Norwegian Sea North Sea Baltic S Benguela Gulf of Thailand South China Sea 15 Modeling process: fitting & drivers Formal estimation Fishing (Diet0) (Z0) ( BCC/B0) Ecosystem model (predation, competition, mediation, age structured) Climate Nutrient loading Predicted C, B, Z, W, diets Log Likelihood Observed C,B,Z,W, diets Habitat area Search Judgmental evaluation Choice of parameters to include in final estimation (e.g., climate anomalies) Error pattern recognition 16 Confounding of fishery, environment, and trophic effects: monk seals in NWHI Fishing effort: Initial Ecosim runs: fishing & trophic interactions together could not explain monk seal decline. Predicted lobster recovery Satellite chlorophyll data indicate persistent ~40% decline in primary production around 1990. ‘Explains’ both continued monk seal decline and persistent low lobster abundance 1970 2000 Low Chl 17 Are seals causing fish declines in the Georgia Strait? Is it fishing? Is it environmental change? Or, is it all three? 18 1950 2000 1950 2000 Strait of Georgia 1.25 31.6 Model Phytoplankton Race Rocks Salinity 31.4 31.2 1.05 31.0 salinity (‰) production anomaly 1.15 0.95 30.8 0.85 0.75 1950 30.6 30.4 1960 1970 1980 1990 2000 • EwE PP & Index of Fraser River runoff (March19 April salinity at two measuring stations) Dave Preikshot, UBC FC BC Shelf biomass changes herring EwE herring SA 4.0 P. cod EwE P. cod SA 0.5 0.5 2.0 biomass (t/km2) 3.0 biomass (t/km2) 0.3 sablefish EwE 1.0 0.2 0.0 1950 0.1 1950 sablefish SA 1970 1980 1990 2000 1960 1970 1980 1.0 0.5 biomass (t/km2) biomass (t/km2) 0.5 1980 2000 1990 1960 1970 1980 1990 2000 seals EwE seal SA 0.08 1.0 0.5 0.3 chinook EwE chinook B from catch 0.0 1950 1960 3.0 hake EwE hake SA 1970 1980 1990 0.0 1950 2000 1960 1970 1980 1990 2000 POP EwE POP SA 0.5 biomass (t/km2) 0.4 0.06 0.04 biomass (t/km2) biomass (t/km2) 1970 1.5 0.3 2.0 1.0 0.02 0.00 1950 1960 0.8 0.2 biomass (t/km2) 2000 coho B from catch 0.4 0.10 1990 0.0 1950 coho EwE halibut EwE halibut SA 0.1 1950 0.2 0.1 sablefish B=C/F 1960 0.3 0.3 0.2 0.1 1960 1970 1980 1990 2000 0.0 1950 1960 1970 1980 1990 2000 0.0 1950 20 1960 1970 1980 1990 2000 Dave Preikshot, UBC FC biomass (t/km2) 0.4 0.4 BC shelf: Upwelling index in May, June, and July. ≥10 year period -20 Model Phytoplankton 54ºN Upwelling 1.1 -10 0.9 0 0.7 1950 10 1960 1970 1980 1990 2000 upwelling (m3/100m/s) production anomaly 1.3 21 Dave Preikshot, UBC FC Northeast Pacific biomass changes 5 arrowtooth EwE 0.6 0.4 3 1960 1970 1980 1990 1 1950 2000 0.8 halibut EwE 1960 1970 1980 1990 0.3 0.4 1960 1970 1980 plaice EwE 1990 2000 POP EwE POP SA 1.2 halibut SA 0.2 0.6 biomass (t/km2) biomass (t/km2) biomass (t/km2) 0.6 0.0 1950 2000 plaice SA 0.4 0.1 1970 1980 1990 0.2 1950 2000 0.8 sockeye EwE 1960 1970 1980 1990 biomass (t/km2) 0.4 0.2 0.4 0.5 chum EwE chum B from catch sockeye B from catch 0.8 0.0 1950 2000 0.4 biomass (t/km2) 1960 0.6 biomass (t/km2) P. cod SA 0.8 0.2 0.4 0 1950 P. cod EwE 2 0.2 0.0 1950 1.0 4 biomass (t/km2) biomass (t/km2) arrowtooth SA 1.2 pollock EwE pollock SA biomass (t/km2) 0.8 0.6 0.4 1960 1970 1980 1990 1980 1990 2000 pink EwE pink B from catch 0.3 0.2 0.1 0 1950 1960 1970 1980 1990 2000 0.2 1950 1960 1970 1980 1990 2000 0 1950 1960 1970 22 2000 Dave Preikshot, UBC FC Northeast Pacific: PDO index (Pacific Decadal Oscillation), April to July. 50 year period 1.5 Model Phytoplankton PDO index 1.0 1.3 0.5 1.1 0.0 0.9 0.7 1950 PDO index production anomaly 1.5 -0.5 -1.0 1960 1970 1980 1990 2000 23 Dave Preikshot, UBC FC Why have Steller sea lions declined? 24 Guenette, Heymans, Christensen & Trites (CJFAS Nov 2006) Alaska Fishing Aleutian Islands Predation Abundance 40,000 Competitive Interactions 30,000 20,000 10,000 0 1960 Ocean Climate Change 1980 2000 Guénette, Heymans, Christensen & Trites (MS) General finding: multiple factors impact ecosystem resources (in all but the easiest cases) Evaluating trends 1. 2. 3. 4. Fishing pressure Trophic impact, including competition Environmental impact Nutrient loading As a rule: All of the above contribute 27 Are we finally able to develop useful predictive models for ecosystem management? • It’s beginning to look like it; • We can with some credibility describe agents of mortality and trophic interdependencies; • Evaluation of relative impact of fisheries and environmental factors is progressing; • As a rule we need to invoke fisheries and environmental drivers to fit models. • When we have a model that can replicate development over time we can (with some confidence) use it for ecosy stem -based policy exploration. 28 Report card: Using models to address ecosystem management questions CONCERN Bycatch impacts GRADE COMMENT We are not bad at predicting direct Aeffect of fishing in general C Trophic effects of fishing can be classified as ‘top down’ or ‘bottom up’ with respect to where management controls are exerted - on valued prey B Changes in M for prey species already subject to assessment - on ‘rare’ prey F Outbreaks of previously rare species Top-down effects (of predator culling or protection) 29 Modeling report card (cont.) CONCERN Bottom-up effects (effects of prey harvesting on predator stocks) Multiple stable states Habitat damage Selective fishing practices/policies Production regime changes Regime shifts GRADE COMMENT Uncertainty here is about flexibility of C predators to find alternative food sources when prey are fished B ‘Cultivation-depensation’ mechanism appears to be main mechanism that could cause ‘flips’ D Lack of understanding about real habitat dependencies, bottlenecks F We have not yet looked closely at options in this area! B Models look good when fitted to data, but have not stood test of time C Policy adjustments in response to 30 ecosystem-scale productivity change So are ecosystem models actually used for fisheries management? 31 Use of EM for fisheries management • Multispecies models – Estimating predation mortality for stock assessment; – Limit harvest of prey species to meet consumer demands; – Impact of changing mesh size, North Sea roundfish; – Minke whale and harp seal culling? – Environmental Impact Assessment (EIA), Alaska groundfish; – Target species response to TACs, Bering Sea. 32 Use of EM for fisheries management • EwE – – – – – – – – – – – Evaluate impact of shrimp trawling, GoCalifornia; Evaluate impact of bycatch, GoCalifornia; Evaluate impact of predators on shrimp, GoMexico; Demonstrate ecological role of species, GoMexico; Impact of proposed fisheries interventions, Namibia? EIA of proposed fisheries interventions, Bering Sea; EIA of alternative TAC’s, Bering Sea and GoAlaska; Target species response to TACs, Bering Sea Closed area sizing, Great Barrier Reef, Australia Valuation of cormorant impact, Ortobello, Italy South Africa pelagic fisheries: in progress. 33 So why aren’t ecosystem models used more for management? • Lack of experience using ecosystem models for predictive purposes; • Ecosystem modeling is for strategic management, and supplements the tactical single species assessment; • Fisheries management process is trapped in tactical management; • Strategic decisions are virtually non-existing. 34 Data gap for modeling • We need longer-term data than typical in assessments to avoid shifting baselines, e.g., 1950-present; – Data mining is required; – There is much more information out there: Catches, CPUE, w, … • Assessments should be expanded back in time: – Stock Reduction Analysis; • Biggest information gaps for: – Mid-TL forage fishes; – Novel conditions (vampires in the basement) 35 – Estimates of mortality rates. Our empirical knowledge is limited • Habitat and environmental changes (including those caused by fishing) and intensive fishery removals are creating novel situations, which we can only handle with difficulty: – We do not to understand the ‘mechanics’ of ecological response well enough to be able to predict all important responses to these novel situations; – Make models one can play with; 36 Our capability to provide advice about large-scale dynamics is limited • We cannot resolve uncertainty about how ecosystems change based on models and time-series data only; 37 Predictive approaches are uncertain, for some obvious reasons • Lack of long-term monitoring data on non-target species and life stages; • Concentration of interaction effects (trophic, habitat) on early life stages (recruitment) that are difficult to monitor; • Confounding of fishery, environmental, and trophic effects in historical data; • Failure to anticipate new problems (‘vampires in the basement’) due to unpredictable changes in system structure, (exotic invasions, fisheries inventions); • Unpredictable pre-adaptations to habitat alterations. 38 Ecosystem modeling for adaptive management requires a very different approach to assessment • Modelers must attempt to uncover alternative models that equally well explain historical data but imply different policy choices: – Environmental vs. fisheries vs. trophic effects; • Policy options would include diagnostic management experiments to distinguish between the alternative models: – Spatial closures to test recovery predictions; – Ecosystem modification to test trophic interaction effects. 39 Models are not like religion – you can have more than one 40 The new Ecopath with Ecosim • Four year project funded through Lenfest Ocean Program • Lenfest Ocean Futures Project: – New generation of EwE to be released Sep 07 – Single-player game version 2008 – Multi-player game version 2009 • Customized versions facilitated • User Ownership 41