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Biological and environmental factors influencing recruitment success of North Sea demersal and pelagic fish stocks Alan Sinclair Fisheries and Oceans Canada Pacific Biological Station, Nanaimo, BC Laurence Kell and Georgi Daskalov CEFAS Lowestoft Laboratory, UK Motivation North Sea stocks are assessed on a single stock basis • However fishing fleets exploit a range of species – For example cod are taken by many gears and as a bycatch in various non-target fisheries. • It is important therefore to look at whether stocks vary together and how environmental factors influence the main commercial fish stocks • Since this has important implications both for yields to the various fishery sectors and for the management of the North Sea fisheries The Main Question Clearly there must be spawners (S) to have recruits (R) – However, inter-annual variability in recruitment far outweighs variability in spawners How Do Environmental Conditions Affect Recruitment? • Do environmental conditions determine – the number of recruits, regardless of spawning stock size? – or the juvenile survival rate (R/S)? • Is recruitment affected by biological processes such as predation, competition or spawning condition? • Is recruitment affected by physical processes such as temperature, salinity …? Main North Sea Commercial Stocks herring 1.0 0.5 0.0 0 1.5 2.5 2.0 3.0 sandeel 1.5 2.0 2.0 1.0 0.5 0.0 0.0 0.0 0.5 0.5 1.0 1.0 1.5 1.5 1.0 0.5 3.0 2.5 saithe 2.0 2.5 plaice 0.0 3 2 1 0 1.5 1.0 0.5 3.0 0.0 2.5 0.0 2 0.5 1.0 4 1.5 1.5 6 2.0 2.0 2.5 haddock 8 cod 0.5 1.5 1.0 2.0 4 0.0 1.5 1.0 0.5 0.0 2.0 whiting 0.0 1 0.5 2 1.0 3 1.5 sole 0 Plaice Sole Cod Haddock Saithe Whiting Sandeel Herring Recruitment • • • • • • • • 2.5 North Sea Species Stock/Recruitment 0.0 0.5 1.0 1.5 2.0 0.0 0.5 1.0 1.5 Spawning Biomass 0.0 0.5 1.0 1.5 Species Likelihood Ratio cod 16.93 haddock 0.05 herring 32.43 plaice 1.36 saithe 1.66 sandeel 0.07 sole -0.06 whiting 3.78 2.0 Stepwise Analysis of Environmental Effects Using Likelihood Ratio Test Null: Recruitment varies around a mean R e Recruitment is density dependent Following a BH relationship S R e S 2 Recruitment is density dependent With an Environmental Component 2 Recruitment is density independent With an Environmental Component R e /2 S E R e S 2 / 2 /2 E 2 / 2 R = recruitment S = spawning stock biomass E = environmental covariate α = maximum recruitment β = biomass at ½ max recruitment κ = environmental parameter σ = residual standard deviation Biotic Hypotheses • Competition / Predation – Recruitment of one species is negatively affected by R or S of another species in the year of spawning. • Juvenile feeding – Recruitment of a pisciverous juvenile (cod, plaice, saithe, whiting) is positively affected by R of a suitable prey species (herring, sandeel) in the year of spawning. • Feeding and spawning fitness – Recruitment of cod, haddock, plaice, saithe, sole or whiting is positively affected by R of any species in the year prior to spawning. – Recruitment of cod, saithe or whiting is positively affected by S of herring or sandeel in the year prior to spawning. Abiotic Hypotheses • North Atlantic Oscillation (NAO) – A single annual mean NAO index was used – Positive or negative effect of NAO on recruitment • Temperature – May act on different part of life history, therefore temperature variables were created from monthly time series and from North Sea sea surface temperature (SST) – Effect of temperature variables may be positive or negative Temperature Variables • SSTY – Sea surface temperature annual mean anomaly • Q1Y, Q2Y, Q3Y, Q4Y – Quarterly mean anomalies in year of spawning • Q1Y-1, Q2Y-1, Q3Y-1, Q4Y-1 – Quarterly mean anomaly in the year prior to spawning • SSTDJF: – Mean winter anomaly, Dec Y-1, Jan Y, Feb Y; • SSTFJ – Mean anomaly Feb – July • PC1, PC2, PC3 – First 3 principle components PCA of Monthly Sea Surface Temperature PCA Monthly Sea Surface Temperature First 3 Components 0.75 Y 0.50 PC1 0.25 PC2 0.00 PC3 -0.25 -0.50 Month Sep Oct Nov Dec May Jun Jul Aug -0.75 Jan Feb Mar Apr Eigenvector • PC1 ~ 54% of Variance – annual signal • PC2 ~ 16% of Variance – contrast between first and second half of year • PC3 ~ 10% of Variance – contrast between summer and winter temperature Results A preliminary first cut at an analysis of this type A broad look at how the North Sea commercial fish species vary together and the possible mechanisms Cod 1963-2002 Model Base Sigma Alpha Beta 0.668 1.012 BH 0.541 2.929 1.765 BH + PC1 0.436 1.053 0.142 Term Estimate PC1 -0.170 Chi p 16.926 0.0000 17.135 0.0000 • Recruitment density dependent • Negative effect of SSTemp (PC1) on recruitment – this has been noted by Planque and Frédou 1999 among others α = maximum recruitment β = biomass at ½ max recruitment Cod 1983-2002 Model Base Sigma Alpha Beta 0.610 0.674 BH 0.535 4.636 3.325 BH + R1San 0.356 3.066 4.421 BH + PC1 0.450 0.867 0.018 BH + R1San + PC1 0.335 0.873 0.586 Term Estimate Chi p 5.266 0.0218 αR1San = maximum recruitment 0.582 16.277 0.0001 β = biomass at ½ max recruitment PC1 -0.188 6.862 0.0088 R1San PC1 0.497 -0.086 11.869 2.453 0.0006 0.1173 • Positive effect of Sandeel Recruitment (R1San) and negative effect of SST (PC1) • The PC1 term not significant in model with both terms • The stock/recruitment parameters are very sensitive to the environmental effect • Resolving which environmental effect is operating is important for interpreting stock/recruitment dynamics Haddock 1963-2002 Model Base Sigma Alpha 1.079 0.981 Term Estimate Chi p R1Sol 0.953 1.592 R1Sol -0.617 9.925 0.0016 S1Her 0.978 1.600 S1Her -0.646 7.826 0.0052 R1Sol + S1Her 0.910 1.979 R1Sol S1Her -0.474 -0.435 5.785 3.686 0.0162 0.0549 • Cannot reject density independent recruitment hypothesis (i.e. no evidence of a significant stock recruitment relationship) • Negative effect of sole recruitment (R1Sol) and herring spawning biomass (S1Her) • The S1Her term not significant in model with both terms • High residual standard deviation (Sigma) regardless of model Sole 1957-2002 Model Base Sigma Alpha 0.770 1.001 Term Estimate Chi p PC2 0.681 0.954 PC2 0.276 11.254 0.0008 R1Pla 0.694 0.483 R1Pla 0.673 9.596 0.0020 PC2 + R1Pla 0.634 0.549 PC2 R1Pla 0.224 0.518 8.207 6.549 0.0042 0.0105 • Cannot reject density independent recruitment hypothesis Positive effect of contrast in SST between winter and summer (PC2) • Positive effect of plaice recruitment (R1Pla) • Both effects significant in 2-parameter model Herring 1967-2002 Model Base Sigma Alpha Beta 0.924 1.077 BH 0.632 2.568 0.962 BH + S1Sai 0.530 3.092 0.323 Term Estimate S1Sai -0.785 Chi p 27.396 0.0000 12.626 0.0004 • Recruitment density dependent • Negative effect of Saithe spawning biomass (S1Sai) on recruitment Plaice Model 1957-2002 Base Sigma Alpha Term Estimate Chi p 0.417 0.992 SSTFJ 0.371 1.053 SSTFJ -0.385 10.673 0.0011 1983-2002 Base 0.471 1.003 R1San 0.401 0.680 R1San 0.359 6.380 0.0115 SSTFJ 0.370 1.275 SSTFJ -0.617 9.642 0.0019 R1San + SSTFJ 0.336 0.938 R1San SSTFJ 0.240 -0.496 3.815 7.077 0.0508 0.0078 • Cannot reject density independent recruitment hypothesis • Negative effect of SSTemp Feb-Jun (SSTFJ) for 1957-2002 and 1983-2002 periods • Positive effect of Sandeel recruitment (R1San)for 1983-2002 period • Sandeel recruitment not significant (barely) in model with both Summary of Biological Effects Hypothesis Comp/Pred Juv Surv feeding Covariate Recruits cod haddock herring plaice saithe sandeel sole whiting Spawners cod haddock herring plaice saithe sandeel sole whiting Recruits Dependent Variable cod haddock - herring sandeel + + cod haddock herring plaice saithe sandeel sole whiting Spawners herring sandeel + + + + + + + + + Spawning Fitness Recruits year before spawning herring - plaice saithe sandeel sole whiting A very large number of plausible biological hypotheses were tested involving competition, predation, - and feeding of feeding of- juveniles - It was- surprising spawners. how -little evidence to support any -was found - of these. - + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + Summary of Temperature and NAO Effects Hypothesis Temperature NAO Covariate pc1 pc2 Feb-Jun Q1 Q4 Q3 Q4 Dec-Feb Annual Q1 y-1 Q2 y-1 Q3 y-1 Q4 y-1 NAO Dependent Variable cod haddock ± ± ± ± ± ± ± ± ± ± ± ± ± ± ± ± ± ± ± ± ± ± ± ± ± ± ± herring ± ± ± ± ± ± ± ± ± ± ± ± ± plaice ± ± ± ± ± ± ± ± ± ± ± ± saithe ± ± ± ± ± ± ± ± ± ± ± ± ± sandeel ± ± ± ± ± ± ± ± ± ± ± ± ± sole ± + ± ± ± ± ± ± ± ± ± ± ± whiting ± ± ± ± ± ± ± ± ± ± ± ± ± ± ± ± ± ± ± Temperature effects may be important for cod, plaice and sole recruitment. For cod and plaice the effects are negative and related to annual or seasonal temperature values. For sole, recruitment was best in years with high seasonal contrast in temperatures. The NAO did not enter in any of the ‘best’ models. However, there is a strong correlation between the NAO and SST, especially SST in the first quarter. Thus, colinearity may be masking important relationships with NAO. Summary and Additional Questions • Why do there appear to be so few significant relationships • Is there ancillary information to support the findings through diets, laboratory study, earlier publications, etc.? • Are some of the ‘significant’ relationships obviously spurious or at odds with accepted conditions in the North Sea? • Are there other mechanisms that should be investigated? – For example, is it temperature or Sandeel that affects cod recruitment? • What are the implications of specific ‘environmental’ relationships for management targets and limits