Spatial differences in biological characteristics of Loligo forbesi (Cephalopoda: Loliginidae) in the Northeast Atlantic

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International Council for the Exploration of the Sea CM 4/CC:3 Cephalopod Stocks: Review, Analysis, Assessment, and Sustainable Management. (Session CC) Spatial differences in biological characteristics of Loligo forbesi (Cephalopoda: Loliginidae) in the Northeast Atlantic Thomas M., Challier L., Santos M.B., Pierce G.J., 3 Moreno A., 3 Pereira J., 3 Cunha M.M., 4 Porteiro F., 4 Gonçalves J. and,* Robin J.P. Laboratoire de Biologie et Biotechnologies Marines, I.B.F.A., Université de Caen, Esplanade de la Paix, 43 Caen cedex France Department of Zoology, University of Aberdeen, Tillydrone Avenue, Aberdeen AB4 TZ, UK 3 INIAP/IPIMAR Av. Brasilia, s/n 4-38 Lisboa, 4 University of the Azores, Department of Oceanography and Fisheries, PT-99 Horta, Azores, * robin@ibfa.unicaen.fr Abstract: Biological data collected in Loligo forbesi during a series of EU funded programs were analyzed using a common set of statistical tools to evaluate large scale variation in the Atlantic. Monthly samples collected in Scotland, English Channel, and Azores and analyzed with similar protocols enabled to record a common set of basic biological variables (length, weight, sex, sexual maturity stage, gonad weight and reproductive system weight). In each area, basic variables are used to compute compound variables which describe the relationship between biological variables (like parameters of the length-weight relationships, or length-at-maturity) the seasonal variation of indices (like sex-ratio, proportion of maturity stages or average gonado-somatic index) and the synchronicity of life history (like the number of months with a majority of mature -or immature- specimen in the population). Differences in length-weight relationships were studied with ANCOVA-like methods. Length-at-maturity were estimated via GLM procedures fitting a logistic function with binomial errors. Seasonal variations in sex ratio and proportions of maturity stages were tested with Chi-square tests and other temporal aspects of life history were compared with non-parametric tests. Significant geographical differences were discussed in the light of published population life-cycles, latitudinal gradients and genetic differences between Azores and continental shelf populations. Key-words: Loligo forbesi, biological samples, statistical differences, geographical comparisons.

. Introduction Biological characteristics of the common squid Loligo forbesi have already been presented in a number of papers, each one devoted to a particular fishing ground (Guerra and Rocha, 994 ; Moreno et al., 994, Pierce et al., 994a ; Porteiro et al., 994). However, published information does not always provide all the elements necessary to test statistical differences across the species range. During the period 989-999 the European Union has funded a series of cephalopod projects (FAR, AIR, FAIR) which included biological sampling of fishery landings. A composite database has been assembled which enables to apply homogeneous statistical procedures to test population parameters. The objective of this analysis is to contribute to the review of Loligo forbesi biological variation. From a fishery point of view biological differences are useful to take into account in the identification of management units. Three biological characteristics - sex-ratio, lengthweight relationships, length-at-maturity relationships - are compared in five different fisheries (Fig. ).. Materials & Methods.. Sex-ratio Chi-square tests are applied to the number of males and females collected with simple random sampling. In addition to the overall sex-ratio per site seasonal differences are sought separately in each area by comparing monthly samples... Length/weight relationships Power models are applied to log-transformed length/weight data for four fishing areas in the Northeast Atlantic. The model is of the form : W = a*l b where W is the weight (in grams) and L is the dorsal mantle length (in millimeters) of a squid. Analysis of variance are performed with the "lm" procedure implemented in S-plus. Linear modeling techniques test differences in origin ordinates (a) and in slopes (b). All models are based on ordinary leastsquares method..3. Length-at-maturity relationships Relationships between mantle length and sexual maturity are only studied in females to avoid problems with the plurimodal length composition observed in mature males. GLM modelling is applied to fit logistic curves with binomial distribution of errors. The regression procedure includes weights which correspond to the number of studied females in each length-class. Fitted lines and 95% confidence intervals are plotted and length-at-5% mature (DML 5 ) confidence intervals are computed using a complementary module (Venables and Ripley, 998). 3. Results 3.. Sex-ratio An overview of spatial differences (Fig. ) indicates that this variable can be biased towards predominance of males. At the monthly scale, deviations from a balanced ratio are either not significant (English Channel) or without clear seasonal pattern (, Moreno et al., 994). Scotland samples suggest predominance of females during periods of breeding activity (Pierce et al., 994a). 3.. Length/weight relationships

In female, allometric coefficients show no statistical difference between sites, except for Scotland and the English Channel (Fig. 4, Table ). Origin ordinates in Scotland are different from all others, maybe due to the higher samples number.l/w relationships in males are significantly different between all fisheries (Fig. 4, Table ). Note that the allometric coefficient is much smaller in Azores squids. 3.3. Length-at-maturity relationships Length at maturity (DML 5 ) does not show significant differences between northern fisheries (Scotland and the English Channel) or between southern fisheries ( and Azores) DML 5 is significantly higher in the south than in the north (Fig. 5). 4. Discussion-conclusion Differences in biological characteristics are difficult to analyze as they can be biased by various problems (fishing gear, sample size, inter-annual trends). Length weight relationships indicate that males from the Azores show much lower allometric coefficient (b) than other samples, this is in agreement with previous morphological studies (Pierce et al., 994b). However, within continental shelf samples differences also occur in a context of genetic homogeneity (Shaw et al., 999). 5. References Guerra A., Rocha F., 994. The life history of Loligo vulgaris and Loligo forbesi (Cephalopoda: Lolignidae) in Galician waters (NW Spain). Fisheries Research, 43-69. Moreno A., Cunha M.M., Pereira J.M.F.,994. Population biology of veined squid (Loligo forbesi) and European squid (Loligo vulgaris) from the Portuguese coast. Fisheries Research, 7-86. Pierce G.J., Boyle P.R., Hastie L.C., Key L., 994a. The life history of Loligo forbesi (Mollusca: Cephalopoda) in Scottish waters. Fisheries Research, 49-63. Pierce G.J., Thorpe R.S., Hastie L.C., Brierley A.S., Guerra A., Boyle P.R., Jamieson R., Avila P., 994b. Geographic variation in Loligo forbesi in the Northeast Atlantic: analysis of morphological data and test of causal hypotheses. Marine Biology 9, 54-548. Porteiro F.M., Martins H.R., 994. Population biology of in Loligo forbesi Steenstrup,856 (Molusca: Cephalopoda) in the Azores : sample composition and maturation of squid caught by jigging. Fisheries Research, 3-4.Shaw P.W., Pierce G.J., Boyle P.R., 999. Subtle population structuring within a highly vagile marine invertebrate, the veined squid Loligo forbesi, demonstrated with microsatellite DNA markers. Molecular Ecology 8, 47-47. Venables W.N., Ripley B.D., 998. Modern Applied Statistics with S+. Second edition, 548 p, Springer-Verlag, New York, 3-45. 3

Table : Regression coefficients and analyse of variance for length/weight relationships of Loligo forbesi female from different fishing areas. Sites n R a Anova b Anova NW Scotland 749.99.7.49 544.98.54.476 English Channel 69.96.64.448 Azores 447.9.74.438 NW Spain 64.97.75.48 P <., no significant Table : Regression coefficients and analyse of variance for length/weight relationships of Loligo forbesi male from different fishing areas. Sites n R a Anova b Anova NW Scotland 554.98.54.459 4.98.6.4 English Channel 656.98.73.35 Azores 6.95.74.53 NW Spain 8.87.83.899 P <., * P <.5, no significant * 4

NW Scotland English Channel NW Spain Azores Figure : Map showing Loligo forbesi sampling locations in Northeast Atlantic fisheries. 5

NW Scotland n= 395 ** English Channel n= 39 -- NW Spain n= 99 ** n= 689 -- Azores n= 78 ** female male % 5% 5% 75% % Figure : Overview of spatial differences in sex-ratio. ** significant deviation from the equilibrium :, -- no significant English Channel 998 cohort : Chi=.84, dl= 6, prob=.9.5 44 66 8 5 5 3.5 6-98 7-98 8-98 9-98 -98-98 -98-99 Figure3: Example of seasonal variation in sex-ratio : the Chi- test indicates no significant difference. 6

.5 8 Scotland Weight (in kg).5 Azores English Channel 6 4.5 Female Male 4 6 5 Mantle Length (cm) Figure 4: Length/Weight relationships of male and female Loligo forbesi from different fisheries. s Proportion of mature animal.5 Azores Scotland English Channel 3 4 5 Mantle Length (cm) Figure 5: Length-at-maturity of female Loligo forbesi from different fisheries. Confidence intervals (95%) are included. 7