The behaviour and spatial distribution of tuna, aggregated beneath fish aggregating devices (FADs), have been studied through ultrasonic tagging experiments but, surprisingly, very few studies on FADs have used underwater acoustic devices. We present techniques, and their limits, incorporating a scientific echo sounder connected to a split-beam transducer to observe and characterise tuna aggregations around FADs, and propose a general approach for future studies. Experiments were conducted in French Polynesia between December 1995 and February 1997. Two methods, echo-counting and echo integration, were used. Echo-counting is possible when individual fish are sufficiently scattered so that each target can be discerned. On the other hand, echo integration can be used with both scattered and aggregated fish schools. The knowledge of tuna target strength is useful for separating targets for echo-counting, and essential for obtaining absolute estimates of densities by echo integration. Sonar performances and settings should be considered when choosing the most suitable method to determine fish density or assessing spatial structure of a tuna aggregation. These techniques allow one to study an entire tuna aggregation, its behaviour in space and time at very fine time–space scales (about a nautical mile and over a few hours), and open up a new scientific field to study the spatial structure and behaviour of tuna aggregations around anchored or drifting FADs.

Despite its wide use in terrestrial ecology, distance sampling is as yet rarely used in underwater visual censuses. The present study attempts to compare density estimators based on distance sampling and on strip transects. Three stations with increasing densities of Chaetodontidae and Pomacanthidae were sampled twice by two divers of unequal experience, using two different transect types. A total of 96 transects and 2970 records of Chaetodontidae and Pomacanthidae were analysed. Nine estimators based on distance sampling were calculated and only the best fit (DT estimator) was kept for comparison with other estimators. These were either based on the average distance of the fish to the transect (AD estimator), or a 3-m- or 5-m-wide strip transect estimator (FW3 and FW5, respectively). There were no significant differences between the means found by DT, AD and FW3. Lower density estimates were given by FW5 in all cases. FW3 and FW5 did not detect several significant differences between stations which were otherwise detected by DT or AD. The number of transects needed to detect a significant difference between stations was four to ten times higher with FW3 or FW5 than with DT or AD. Diver experience was found to be a significant factor in density estimates. However, this factor was less important than the choice of the density estimator. Transect type or the day of sampling had no consequence for the estimates. The distance distributions of fish were divided into three different patterns which may be explained by a combination of detectability function and a behavioural component.

Egg quality is one of the most important factors determining larval viability. The study of oocytes released by ‘wild' broodstock will contribute to the definition of quality criteria applied to hatcheries as well as being an indicator of the oyster reproduction potential and aquaculture ongrowing systems. The aim of this study was to determine the relationship between condition of Crassostrea gigas spp. angulata (Portuguese strain) from ‘wild' broodstock (condition index, gonadal maturity and number of oocyte released), oocyte biochemistry and hatching rate of eggs during the spring/summer of 1995. Stages of gonadal maturity and condition index indicated that natural spawning of this species occurred between April and August with the highest spawning intensity occurring in June. Analyses demonstrated that C. gigas oocyte organic matter consist of 44–74 % proteins, 16–38 % lipids and 7–12 % carbohydrates. A significant relationship was observed between some biochemical parameters – organic matter and lipid content – and broodstock condition index and hatching rate. It seems that these two oocyte parameters (organic matter and total lipids) could be used to define quality of oocyte and thus larval viability. The oocyte protein content was also found to be associated with broodstock and larval quality. In summary, these data are a contribution to the knowledge of the reproductive cycle of oysters in Europe and may be useful in improving hatchery management of this species.

Bioassays were carried out with the ‘blue diatom' Haslea ostrearia Simonsen, which is responsible for oyster greening during the fattening period of Crassostrea gigas Thunberg in oyster ponds. Samples of seawater were taken from two oyster ponds: one without oysters and the other with 20 oysters per m[sup2 ], maximal density allowed by the French AFNOR norm for ‘refinement'. The aims were to clarify the nutrient requirements of this diatom, also to elucidate the eventual influence of C. gigas at this density on the seawater fertility and to envisage the mass production of this diatom by pond fertilization. Examination of cell numeric densities at the end of bioassays allows us to conclude that silicate was the first limiting nutrient, closely followed by phosphate. Chlorophyll a concentrations led to different conclusions: phosphate was the first limiting factor, but after the seawater storage period in ponds, seawater quality evolved to a deficiency of nitrogen. Silicate addition increased cell division rate, and silicate depletion increased chl a synthesis for this species. Examination of nutrient assimilation ratios confirms that H. ostrearia requires a large amount of silicon. From these results, it was possible to prepare a N + P + Si simplified medium which has been tested in laboratory and field mesocosm conditions. In both conditions, similar results were observed: a significant increase in H. ostrearia cell concentrations and consequently an evolution up to the greening stage. Applications of this work are numerous; the principal permits us to envisage the production of this species in 25-m3 ponds, with the aim of allowing constant production of the greening phenomenon.

Haemocytes of Mytilus edulis, allowed to attach to the plastic surface of a tissue culture plate in the presence of haemolymph, were observed by time-lapse video recording. When bacteria were added at concentrations of 10 or 50 bacteria per haemocyte, certain bacterial strains caused rounding of the cells within 2–3 h. Haemolymph was necessary for the rounding to occur; if bacteria were added in sterile seawater there was no significant difference in the number of rounded cells between control and bacteria-treated cultures for up to 4 h. The haemolymph factor required for this activity was active at 1/64 dilution in seawater, was sensitive to trypsin treatment, and activity was halved on heating at 56 or 100 °C for 30 min. For the most toxic bacteria tested, Vibrio alginolyticus NCMB 1339 and Vibrio anguillarum A7, haemocyte cell rounding appeared to be induced by a very small number of bacterial cells. Bacteria-free culture supernatant of V. anguillarum 2981 induced rounding of haemocytes in a dose-dependent manner, with 50 % of cells being rounded at a dilution of approximately 1/500 of the culture supernatant. In a survey of 226 bacterial isolates, those isolated from incidents of disease in a bivalve hatchery were significantly more toxic towards haemocytes than bacteria isolated from hatcheries without disease or from turbot hatcheries.