In the Western and Central Pacific Ocean (WCPO), which accounts for over half of world tuna production, purse seine effort and catch on floating objects have increased significantly due to a rapid increase in the use of fixed and free-floating fish aggregation devices (FADs). FAD fishing has had an impact on the current status of the stocks of the three main target tunas in the equatorial WCPO, skipjack (Katsuwonus pelamis), yellowfin (Thunnus albacares) and bigeye (T. obesus). FADs have been shown to influence the behaviour and movement patterns of the three tuna species with the juveniles of each species occupying shallower habitats when associated with FADs. Aggregation of tunas around drifting objects increases their vulnerability to purse seine gear, particularly for juvenile and small size classes. Further to the impacts on the target stocks, the use of FADs has increased the vulnerability of other fishes to the purse seine method, including some shark and billfish species. Given the concern over FAD-related fishing effort on target and bycatch species, there is a need to understand how FAD use affects target and bycatch stocks. Science needs to better support management decisions are highlighted including the need to identify the magnitude of broader community-level affects.

The pole and line tuna fishery in the Maldives relies heavily on an array of 45 anchored fish aggregating devices (FADs), making it one of the largest anchored FAD-based tuna fisheries in the world. We examined the behaviour of skipjack (Katsuwonus pelamis) and yellowfin (Thunnus albacares) tuna around anchored FADs (1 000 to 2 000 m deep) in the Maldives using passive acoustic telemetry. Eight neighbouring FADs (distance range: 30 to 95 km, average: 50 km) were equipped with automated acoustic receivers in January 2009, for a period of 13 months. A total of 40 skipjack (37−54 cm FL) and 21 yellowfin (35−53 cm FL) tuna were tagged with Vemco V13 transmitters in January (start of the northeast monsoon, dry season) and November (end of the southwest monsoon, wet season) 2009 and released at the two central FADs within this instrumented array. No movement between FADs was observed for any acoustically-tagged tuna in the instrumented FAD array. These results suggest that FADs in the Maldives may act independently. The maximum time a tagged skipjack remained associated with a FAD was 12.8 days in January but only one day in November. In addition, residence times at FADs were found to differ with time (month) and space (FAD location) for skipjack tuna, suggesting that external biotic factors (e.g., prey, conspecifics or predators) might influence the time this species spends at FADs. In November, the residence times of yellowfin tuna (maximum observed time: 2.8 days) were three times greater than those of skipjack tuna at the same FADs. This specific difference could be explained either by the two species responding to different factors or by the species’ responses being dependent on the same factor but with different thresholds. No particular preference for time of departure from the FADs was observed. Some monospecific and multispecific pairs of acoustically-tagged individuals were observed leaving the FADs simultaneously. Thus, this study indicates a high degree of complexity in the behavioural processes driving FAD associations.

Catch-at-size data of the eastern Atlantic skipjack were used to estimate changes in total mortality from 1969 to 2007. We used a transitional model of mean length that generalized the Beverton-Holt mortality estimator to allow change in mortality rate under nonequilibrium conditions. Then, from homogeneous periods of time, length-converted catch curves were used to access qualitative changes in selectivity patterns for two surface fisheries (the baitboat fishery operating from Dakar, Senegal, and the European and associated purse seine fisheries). To explore the impact of catch on the mortality rate, a Bayesian change-point analysis was conducted on the catch time series to detect concomitant variation between mortality rates and catch. Finally, potential causes of these changes are discussed in relation to the implementation of new fishing technology, such fish aggregating devices (FAD). The general pattern depicted by total mortality is in agreement with previous knowledge on this fishery: a state of complete or practically complete exploitation during the nineties followed by the decrease in nominal purse seine fishing effort in the last decade, combined with the effect of a seasonal moratorium on FAD fishing operations. There was no evidence of a change in selectivity between the two contrasted periods of time considered: 1969-1979 and 1986-1999; the second period being characterized by the introduction of new technology onboard vessels. In contrast, the covariation over time between total catch and mortality rate three years later highlights the effect of the fishing pressure on the stock of eastern Atlantic skipjack.

In order to assess the latitudinal variability in growth of the eastern Atlantic skipjack (Katsuwonus pelamis), conventional tagging data collected by the International Commission of the Conservation of Atlantic Tunas (ICCAT) since the 1960s are reanalyzed using a modified version of the von Bertalanffy-Fabens growth model. An analysis of the latitudinal patterns of recaptures showed that the lowest mixing rate between northern and southern regions was evidenced at 10° N Latitude. Since it is theoretically admitted that growth parameters L∞ and K are negatively correlated, we substituted L∞ into the growth equation model by a simple bioenergetic function of K fitted from existing studies on skipjack growth parameters. The likelihood for the meta-analysis of growth is combined with the likelihoods from the two regional tagging data with the aim of estimating simultaneously K in both areas and to transfer adequately uncertainties associated with the different data sets. From this study, it was showed that fish inhabiting waters south of 10° N latitude can be expected to grow generally larger but at slower rate than in the North (L∞ = 112.34 cm vs. 89.38 cm, and K = 0.14 vs. 0.38, respectively). Our results are consistent with the range of growth estimates obtained in the Atlantic Ocean and in different parts of the World's oceans. In contrast, the estimates of L∞ and K done in the Senegalese region in the 1980s within the framework of the Skipjack Year Program, and traditionally applied by ICCAT, are not supported by the present study. The findings concerning the phenotypic plasticity exhibited by growth of skipjack among latitudinal regions suggest potential differences in fish population productivity and consequently imply that non-conventional stock assessment methods such as catch-at size/growth transition matrix per region could be used to assess the responses of skipjack to exploitation.

An advection diffusion reaction model was used to estimate movement and tag attrition parameters from skipjack tuna tagging data off the Maldives. Two sets of data were available from the experiments carried out during two distinct periods: 1990–1991 and 1993–1995. The results of the analysis were compared with the previous analyses and discussed in relation to management of skipjack fisheries in the Maldives and in the Indian Ocean. The movements were found to be highly variable in space and time, and few consistent patterns were observed between the two data sets. Similarly, significantly different estimates of fishing and natural mortality rates were observed from the two data sets. These differences were found, in part, to be due to the uneven distribution of tag releases in both space and time. Estimates of movement and attrition rates show that emigration from the Maldivian fishery to the rest of the Indian Ocean’s was small. The exploitation rate was found to be substantial, contributing about 30-40% of the total attrition in the fishery area. Such levels of localized exploitation may be maintained by steady immigration from outside of the Maldives, but more extensive tagging is required to be certain. The impact of tuna fisheries elsewhere in the Indian Ocean on the domestic Maldivian fishery cannot be determined until a comprehensive large-scale tagging program, including all the fisheries in the Indian Ocean, is completed.

Vitellogenin (VTG) levels were measured in the plasma of 143 female skipjack tuna, Katsuwonus pelamis caught in the Western Indian Ocean. These levels were correlated with the gonadosomatic index (GSI) and with plasma 17β-estradiol (E2) levels during the reproductive cycle. VTG and E2 levels were measured using a competitive enzyme-linked immunosorbent assay (ELISA) and a radioimmunoassay (RIA), rcspectively. VTG was purified from a pool of plasma obtained from females with high GSI using a double chromatography method (gel filtration and ion exchange). A specific antibody was obtained in rabbits. The VTG immunoenzymeassay developed gave an assay detection limit (90% binding) of 15 ng.ml-1. Mean VTG levels ranged from 1.2 mg.ml−1 to 4 mg.ml−1. Mean monthly VTG values remained relatively elevated during the resting periods (1.2 mg.ml−1 in April and 1.9 mg.ml-1 in September), while maximum levels reached only 4 mg.ml−1 during the reproductive season. The highest GSI values were observed from November to March during the major reproductive season corresponding to the North monsoon and from early June to late August during the minor reproductive season corresponding to the East monsoon. Lowest GSI values were found in April-May and September-October. Mean E2 levels exhibited considerable variability among all females sampled ranging from 700 pg.ml−1 to 9 ng.ml−1. This study demonstrated that the sexual maturation was correlated with the monsoon seasons and that there was a positive correlation between monthly variations of GSI, VTG and E2 levels in the skipjack tuna population from the Western Indian Ocean.

Un système expert simple, reposant exclusivement sur des statistiques de pêche, a été élaboré afin d'estimer des migrations de poissons entre zones. Les flux de migration par trimestre sont calculés à partir de la comparaison de deux estimations distinctes des effectifs par zone et par âge, la première tenant compte du phénomène des migrations, la seconde non. La première estimation est obtenue en répartissant par zone les effectifs par âge issus d'une analyse des cohortes, la seconde est calculée période par période, à partir des effectifs présents dans chaque zone à l'âge précédent. Le modèle est appliqué au listao de l'Atlantique tropical Est. Les flux de migration estimés sont alors analysés, par groupe d'âge puis pour l'ensemble de la population. Bien qu'un certain nombre de limitations inhérentes au modèle existent, les résultats obtenus apparaissent valides par rapport aux schémas connus des migrations du listao.

Quelques aspects de la reproduction du listao (Katsuwonus pelamis) dans deux zones distinctes de l'ouest de l'océan Indien ont été étudiés de février 1989 à février 1994. A partir d'échantillonnages faits, soit à bord des thoniers senneurs sur du poisson frais (1 656 individus), soit à la conserverie de Maurice sur des thons décongelés (4 152 individus), les différents stades du cycle sexuel ont pu être précisés. La taille de première maturité sexuelle est atteinte à 41–42 cm (longueur à la fourche) chez les femelles et à 42-43 cm chez les mâles, correspondant à des individus âgés d'environ 1,5 an. L'évolution mensuelle de la proportion des différents stades macroscopiques de maturation des gonades montre que, quel que soit le mois considéré, il y a toujours plus de 70 % des femelles échantillonnées qui présentent des ovaires en fin de maturation (stade IV). Les variations du rapport gonado-somatique (RGS) montrent que la reproduction du listao a lieu toute l'année mais qu'il existe cependant plusieurs périodes d'activité sexuelle plus intense. L'observation histologique de 737 ovaires indique la présence de follicules post-ovulatoires (indicateur de ponte récente) pendant les 2 périodes de mousson, mousson de nord-ouest (novembre à mars) et mousson de sud-est (juin à août) tandis que la proportion d'ovaires présentant des follicules atrétiques est maximale aux 2 périodes d'inter-mousson (avril-mai et septembre-octobre). L'étude du sex-ratio montre que. pour l'ensemble de la période d'étude et pour les deux zones considérées, la proportion de mâles est significativement supérieure à celle des femelles. Ses variations mensuelles semblent indiquer une accentuation de la prédominance des mâles à chaque période de ponte plus intense.

La fécondité par acte de ponte du listao Katsuwonus pelamis de l'ouest de l'océan Indien a été étudiée à partir de 281 femelles dont les tailles (longueur à la fourche) sont comprises entre 43 et 73 cm et dont les ovaires étaient à un stade de maturité sexuelle avancé. Le liquide de Gilson, utilisé comme agent conservateur et dissociateur des ovocytes, a une action importante et rapide (5 jours) sur le rétrécissement des ovocytes. Des comptages effectués à l'aide d'une cuve de Dollfus sur des sous-échantillons d'ovocytes dissociés, montrent que pour une même période d'activité sexuelle (février), la fécondité du listao du canal de Mozambique est semblable à celle des listaos du sud du plateau des Seychelles. Bien qu'une activité sexuelle du listao soit notée tout au long de l'année, la fécondité individuelle varie d'une saison à l'autre et ce, pour un même secteur géographique. Cette fécondité individuelle par acte de ponte varie de 80 000 œufs pour des femelles de 44 cm provenant de la côte nord-ouest de Madagascar à 1,25 millions d'œufs pour des femelles de 75 cm pêchées autour des Seychelles. La fécondité relative correspondante évolue donc entre 40 et 130 œufs/g de poids de corps. Pour cette espèce, le nombre de pontes successives a été estimé à 4 par an.