Mortality control of scallop larvae in the hatchery

Larval mortalities occurring in molluscan hatcheries have often been associated with bacterial contamination, and more specifically with vibrios. Although batches of oyster and clam larvae have been routinely reared in the hatchery of Argenton (North Brittany, France) without antibiotics, high larval mortalities have been recorded with the great scallop, Pecten maximus, under similar conditions. For this species, an addition of antibiotics was found necessary and chloramphenicol was used at a concentration of 8 mg l^–1. However, this chemical has now been banned in Europe, making either substitution products or an improvement in the rearing procedures essential. Studies carried out have shown that neither a decrease in larval density (to 1 larva ml^–1) nor an increase in seawater change frequency (to one per day) had any positive effects. Furthermore, elective substances such as sugars were not suitable and the use of another antibiotic, erythromycin, led to inconsistent results. The only positive effects were obtained with lower levels of chloramphenicol, which does not resolve the problem. Because no alternative solutions have as yet been found, further research needs to be undertaken.     

Effects of air emersion on survival and growth of hatchery rearedgreat scallop spat

Scallop spat production normally requires transfer between growthsystems. Simulated transport experiments were carried out in April, June,December and February to evaluate effects of transport time on greatscallop (Pecten maximus) spat growth and survival. The spat (1.7–1.8 mm in shell-height and 21–25 µg ash free dry weight [AFDW]) wereheld in moist coffee filters at a temperature of 10 °C for up to 24 h,before being replaced into sieves in rearing tanks at 15 °C. The studyshowed that by increasing air emersion time, survival and growthdecreased. No significant difference in the results between 0 and 4 h of airemersion was found, while the effects after 12 and 24 h differed betweenspat groups. Survival and growth rates showed seasonal differences. Meansurvival was 35–71% in April and 77–99% from June to February. In Junemean growth rates attained were 115–128 µm shell-height and 15–18µg AFDW per day compared with 49–69 µm and 3.8–7.0 µgper day for the other spat groups. Great scallop spat may survive atransfer time of 24 h, but transportation for longer than 12 h is notrecommended if subsequent high survival and growth rates are to beensured.     

Bacterial nutrition of great scallop larvae

Bacterial nutrition of great scallop, Pecten moximus, larvae was investigated using the radioactive tracer technique. The bacterial labelling was studied initially to obtain a high and stable specific radioactivity (¹⁴C) of bacterial cells. A higher bacterial specific ¹⁴C activity was obtained when the tracer (amino acid) was introduced in the culture medium at the beginning of the exponential growth phase. After a 12 h labelling period in a rich nutritive medium, the bacteria were depurated in seawater for 5 h (chase) to prevent further ¹⁴C excretion and then added to larval rearing vessels. The larval labelling was followed for 12 h and then larvae were placed in new vessels without radioactive bacteria. The depuration of larvae was followed for 3 days. Data obtained on ingestion and assimilation efficiency show that bivalve larvae are able to ingest and digest bacteria.     

Influence of the gametogenic cycle on the biochemical composition of the ovary of the great scallop

The oogenic cycle and biochemical composition of the ovary of raft-cultured great scallop (Pecten maximus) were studied during the period April 1990–July 1991. The ovary condition index (FGI) and stereological studies showed the existence of two principal spawning periods, winter and late spring-early summer. No sexual resting period was found. Oocyte lysis was high throughout the year. Ovarian lipid levels displayed a clear seasonal pattern linked to the gametogenic cycle. Total lipid (TL, 16–21% dry weight), acylglycerol (AG, 20–65% TL) and free sterol (FS, 2.8–6.4% TL) levels were, generally, higher in the ripe ovary and a decrease coincided with spawning. Protein (59–63% dry weight), glycogen (<3% dry weight) and phospholipid (PL, 26–35% TL) levels showed no clear seasonal trend. The TL and AG were a good index of ovarian sexual maturity. The TL % of dry weight) correlated well with the female gonad condition index (r _s = 0.779, p < 0.001), and AG (% f TL) correlated well with the mean oocyte diameter (r _s = 0.630, p < 0.01) and the female gonad condition index (r _s = 0.443, p < 0.05).     

The effect of seawater flow and temperature on metamorphosis and postlarval development in great scallop

Variations in growth and survival of hatchery-reared post-metamorphicjuveniles of great scallop Pecten maximus prompted anexamination of settlement and postlarval development. The effects ofseawater flow and temperature on great scallop metamorphosis andpostlarvae were studied over a 4–5 week period. In allexperiments, and regardless of environmental conditions, great scallopmetamorphosed after a 2–3 week period with values of 35 to70%. Subsequently, spat numbers increased slightly. Spatmortality generally occurred from the third week onward and reachedlevels as high as 30% by the fifth week under standardconditions. At 20 °C, however, 60% mortality levels wererecorded. Differences in spat growth rate, ranging from 37 to 45 mday^–1, were noticed at different seawater flow ratesbut no clear tendency could be discerned. Temperature affected spatgrowth with an increase in size from 24 m day^–1 at15 °C to 35 m day^–1 at 18 °C. Conversely,growth was suppressed at 20 °C (14 m day^–1).For optimal metamorphosis and postlarval development in great scallop, aseawater flow of 4.3 L h^–1 per sieve and a temperatureof 15 °C are recommended.     

A preliminary study of the behaviour and vitality of reseeded juvenile great scallops, of three sizes in three seasons

In order to have a better understanding of recessing in great scallop, Pecten maximus and consequently the causes of mortality at reseeding, this study has monitored, at different seasons, the dispersion and recessing of different sizes of juveniles (about 15, 30 and 45 mm, called small, medium and large) after seeding. Moreover, the aim was to see when small spat (15 mm) could be seeded, and thus reduce the costs of intermediate culture.Three monitoring approaches were used together: (1) continual observations by remote video camera, of a defined area (less than 1 m²) containing 10 scallops from each size group; (2) daily monitoring of behaviour with divers along three bottom lines, with 20 × 1 m² plots each and nine marked scallops per plot; and (3) the biochemical content of the muscle: adenylic energetic charge and storage of energy reserves (glucides, proteins, lipids).The video monitoring identified but did not quantify predator behaviour, particularly at night. The role and behaviour of spiny crab, Maia squinado, and of small predators has clearly been shown, such as: (a) small crustaceans, Inachus sp., breaking the edges of scallop valves; and (b) small gobies, Pomatoschistus pictus, pecking the tentacles of the scallop mantle.For the monitoring by divers, filtering appeared much too difficult to look at for it was very disturbed by divers, and anyway the resumption of filtering came immediately after seeding. On the other hand, diver monitoring of dispersal and recessing was quite easy to do with a minimum of practice. On the basis of dispersal, the best seasons for seeding appear to be spring or summer. In autumn, two-thirds of small and medium juveniles are missing 3 days after seeding, but we could not observe whether they had been eaten by predators or had just moved and recessed farther. There was no experiment in winter owing to adverse conditions for scallop seedings.Biochemical analyses confirmed the unsuitability of autumn for scallop seeding, because of very low glucide content in this season.The adenylic energetic charge in the smooth part of the muscle showed that stress before seeding (aerial exposure, handling), and post-seeding behaviour (swimming, recessing) have a high energetic cost for scallops. In summer and autumn, 3 days after seeding, none of the three size batches recovered their initial vitality.     

Seasonal differences in effect of broodstock diet on spawning success in the great scallop

Great scallop (Pecten maximus L.) broodstock collected at two different seasons, spring (May) and winter (December), were given four different diets during conditioning. The spring group was spawned in late June, and the winter group in February.The highest number of veligers in the summer spawning (30 millions per 10broodstock), was produced using a diet consisting of 80% Tahitian Isochrysis galbana. In the winter spawning, broodstock given a dietconsisting of 80% diatoms (Skeletonema costatum/Chaetocerosgracilis) produced the highest number of veligers (29 millions per 10broodstock). Fecundity and the number of egg-releasing individuals were higher in the early summer spawning (June) than in the winter spawning (February), however, the total number of three days old veligers produced was nearly the same in the two seasons.     

Post-transport recovery of cultured scallop (<Emphasis Type="Italic">Pecten maximus</Emphasis>) spat,juveniles and adults

High mortality associated with transport operations in scallop culture has been a major problem faced by European farmers. Simulated transport with Pecten maximus L. spat <2 mm, spat 15–30 mm, juveniles 30–50 mm and adults >100 mm were carried out in Spain, Ireland and Norway. Different time and temperature combinations were studied in order to maximise post-transport survival and establish best practices. Out-of-water transport could result in 100% survival if conditions were right, but the response to emersion stress depended on size, season and location. Post-transport recovery decreased with emersion time and was strongly influenced by temperature. Air exposure was tolerated for a longer time by adult scallops than spat and juveniles, but the results differed among trials in the different countries. The maximum emersion time that gave post-transport survival ≥80% was 12 h for the smallest spat, 18 h for larger spat and 24 h for juvenile and adult scallops. Adults were less affected by transport temperatures that deviated from ambient seawater temperature than spat and juveniles. In general post-transport recovery was high when sea temperature was <10°C, but during warm-water seasons special care should be taken to avoid stressful and lethal transport conditions. A transport temperature <12°C was recommended, though not more than 10°C below ambient culture temperature. A maximum transport time of 9 h was suggested for spat and juveniles to attain post-transport survival close to 100%, but 12–24 h was feasible during the cold-water season or at favourable transport temperatures.     

Vitamin requirements in great scallop larvae

Vitamins were analysed in food (microalgae) and larvae of great scallop, Pecten maximus, during larval development. Microalgae used to feed larvae in hatcheries show great variability in their vitamin composition depending on both the species and culture condition (phase of growth). The microalgae used to feed Pecten maximus larvae were rich in vitamins; their content compared with diets used in fish culture appeared sufficient, with the possible exceptions of pyridoxine, biotin and pantothenic acid. Vitamins in bacteria, isolated from the larval rearing tank were also analysed, as they can also contribute to the diet. Vitamin B₁₂, -tocopherol and -carotene were detected in very low concentration in bacteria; however, some bacterial strains were rich in pantothenic acid, and the pattern of other vitamins was similar to that from microalgae. The presence of bacteria can complement the diet in panthothenic acid, as it has been demonstrated that bacteria are ingested by larvae. The vitamin content of Pecten maximus larvae was analysed from the second day after hatching to just before metamorphosis. The content of some vitamins, ascorbic acid (C), -tocopherol and -carotene, increased during larval development, suggesting that their requirement was satisfied. However, thiamin and riboflavin decreased during larval development and further studies, possibly using microencapsulated vitamins supplements, are needed to determine whether these vitamins are limiting during larval development.     

Great scallop, Pecten maximus, research and culture strategies in Norway: a review

The great scallop, Pecten maximus is a potentialaquaculture species in Norway, but production to date has been low. Greatscallop landings in 2000 were 571 tonnes, exclusively from harvesting wildstocks, landed by divers. Approximately two million juveniles of 15mm shell height have been produced annually in a hatchery since1998, and distributed to farmers. Research projects on larvae and juvenilesinclude studies of various antibacterial treatments, improved culture systemdesigns and application of probiotics. Results from hanging cultures underdifferent environmental conditions indicate a strong correlation between lowtemperature and poor survival, and point out the importance of careful selectionof cultivation sites. Good growth potential of scallops in Norwegian waters hasbeen shown, and it is possible to reach market size of 10 mm shellheight in three to four years. Experiments with fences and other strategiesprotecting cultured scallops on the seabed from predation by crabs are inprogress.     

Fatty acids and egg quality in great scallop

Spawners of the great scallop, Pecten moximus, were conditioned on three microalgal diets: T-Isochrysis, a mixture of four species (PTSC) and Chaetoceros calcitrans.The polyunsaturated fatty acid (PUFA) composition of neutral and polar lipids of eggs was related to the fatty acid composition of the diet. However, the 20 and 22 carbon PUFAs were maintained at significant levels independent of those of the diet when these fatty acids were present in the diet at low levels. This effect was more pronounced in the polar than in the neutral lipids. A preferential incorporation of 22:6(-3) and 20:4(-6) was demonstrated in the polar lipids. This emphasizes their role in ovogenesis and embryogenesis.The 22:6(-3) requirement of P. maximus was better satisfied by T-Isochrysis, which favoured the highest incorporation of this essential fatty acid in the eggs. The good success in reproduction obtained with this monospecies diet led us to modify multispecies diets by increasing the level of 22:6(-3).     

Abnormal melanization and microstructural distortions of the shell of great scallop living in shallow water

Modifications of great scallop (Pecten moximus) shells have been noticed in many sites of scallop fisheries in Brittany, especially in shallow waters. These calcification abnormalities are linked to the appearance of a brown colouration of the internal calcified shell layer, due to the presence of a eumelanin associated with the insoluble organic matrix of the biocrystals. The appearance of this pigment generates many disturbances of the calcified foliated microstructure of the scallop internal shell layer. The mantle structure is not modified in brown shells as compared with white ones. No pathogenic signs such as hyperplasia or haemocytic infiltration have been observed. According to this observation, we hypothesize that the brown colour phenomenon is more a result of environmental disturbance rather than a symptom of a pathogenic disease.The colour abnormalities of the internal shell layer can be detected by a spectral analysis of its reflectance before it can be detected with the naked eye. This method, correlated to microstructural observations, gives a rapid and precise analysis of the appearance of the pigmentation on adult or juvenile scallops. It may be a useful method for the evaluation of the influence of environmental parameters, for example, on calcification and its abnormalities.     

Effect of air exposure on scallop behaviour, and the implications for subsequent survival in culture

Scallop spat produced for continued culture normally requiretransportation between sites, and the associated stresses may causemortalities. In the present experiment, scallops of 40–55 mm shell heightwere emersed in air for time intervals up to 24 h and their behaviourexamined once re-immersed. Scallops were placed upside-down and thenumber of movements and the cumulative numbers righting in 5 min timeblocks were recorded. The greatest frequency for all behaviouralresponses was found at 15–17 °C in August. Responses were reducedin November and June (9–11 °C) and least at 5 °C in January.All effects of treatment, temperatures and season, and increases in airexposure were significantly different. Following the treatments, mortalitiesafter 10 days in culture was about 10–30% for scallops emersed for 18 and24 h in August and June. Scallops did not show significantly differentbehaviour whether they were emersed upright or inverted. However,scallops emersed at 15 °C had fewer responses than scallops held at <10 °C, so chilling during transport may prolong scallop vitality. Theresults suggest that air exposure >12 h should be avoided. At temperatures>9 °C, behavioural responses may be a simple and effective method toassess vitality which can assist in the management of scallop culture.     

Growth and mortality of the king scallop grown in suspended culture in Malaga, Southern Spain

Growth and mortality of the king scallop, Pecten maximus, werecompared when grown in cages and by ear hanging in suspended culturein Fuengirola, Malaga, in southern Spain. Seed (juveniles) used in theexperiment was collected in September 1997 that had settled on collectorsin April-June, of that year. Culture in suspended cages began in January1998 when the seed measured 42.7 (3.3) mm shell height and ended inFebruary 1999. Significantly faster growth was found at a minimum culturedensity (16 scallops/cage) than at two other densities (24 and 36scallops/cage). Depth (1, 5 and 10 m from the bottom) influenced growth,poorest growth occurred closest to the bottom. Under optimum growingconditions, 16 scallops/cage suspended 10 m from the bottom, scallops grewto 10 cm shell length (legal size) by February 1999.In ear hanging culture, ropes were moored in April (51.3 (4.5) mm),June (58.2 (4.5) mm) and November 1998 (64.3 (4.9) mm).Initially, rapid shell growth was observed in all three cultures.Subsequently, the shells became covered with barnacles, Balanus sp.,that possibly caused total mortality of the April culture and led to highmortalities in the two other cultures.     

Yields of great scallop, Pecten maximus, larvae in a commercial flow-through rearing system in Norway

Survival, growth and yield of competent great scallop (Pecten maximus) larvae were investigated during a full production season in a commercial hatchery in western Norway. Broodstock were collected from natural scallop beds and 12 groups were induced to spawn during the period December 2002 to July 2003. Larvae were reared on a large scale in 36 flow-through tanks (3500 l) at 17±1 °C and continuously fed a mixture of five algal species produced in an indoor continuous-flow system. Large variations in larval performance between spawning groups and tanks were observed, but the results were as good as earlier results using the batch system and prophylactic addition of chloramphenicol. Growth from days 3–24 averaged 4.8 μm day⁻¹±0.8 (sd) and survival 22.4%±21.8 (sd). Mean yield of day 3 larvae was 7.1%±10.0 (sd) and 26.6%±25.9 (sd) for those surviving to day 24. Yield was significantly correlated to larval survival. Larval success was related to initial larval density, algal concentration and season. It was found that the best production regime had an initial larval density lower than 6 ml⁻¹ and algal concentration of less than 12 μl⁻¹ regardless of season. Seventeen tanks met these criteria and produced a mean yield of 0.5 larvae ml⁻¹ to settlement. Flow-through systems are currently regarded as the only feasible method for viable hatchery production of P. maximus larvae in Norway.     

Effect of photoperiod on conditioning of the great scallop

A 45 days experiment was conducted by exposing adult scallops with empty gonads to three different photoperiod regimes under constant food and temperature conditions: Simulated natural/decreasing photoperiod (N), constant photoperiod (C) and increasing photoperiod (I). At the end of the experiment the I and C groups had significantly higher gonad indexes and larger oocyte diameters compared to the N group. No significant changes were found in the N group during the experiment. The adductor muscles and digestive glands did not change significantly during the experiment and no differences were found between the groups. These results suggest that photoperiod affects early rebuilding of gonads in scallops from Western Norway.     

Influence of season, initial size, depth, gear type and stocking density on the growth rates and recovery of sea scallop, Placopecten magellancius, on a farm-based nursery

Hatchery-reared sea scallop (Placopecten magellanicus) spat weremonitored for growth and recovery in three experiments to determine themost suitable system for nursery culture. In Experiment I, four size classesof nursery-sized spat held at two depths from October to July exhibiteddeclining growth rates over the winter period and increased growth ratesin the spring. Overall, season, depth and initial size had a significantinfluence on the absolute and specific growth rates of scallops. Recovery,defined as number of scallops remaining after mortality and loss of spatthrough gear mesh, was influenced by season and initial size, but notdepth. Scallops in the 3.0 mm⁺ size class had higher growth rates andrecovery than those in the 1.4–1.6 mm, 1.7–1.9 mm and 2.0–2.9 mm sizeclasses. In Experiment II, two gear types containing similar size spat werecompared. Growth rates were significantly higher in 3.0 mm pearl nets thanin 3.0 mm collector bags, although recovery was similar between the twoequipment types. Experiment III, two stocking densities of nursery-sizedspat were compared in collector bags. Neither growth rate nor recoverywere significantly different for the two densities (2600 and 5200spat/collector bag) tested. Overall, these studies indicated that importantparameters for optimizing the growth and recovery of scallops in a farm-based nursery system include season, initial spat size, deployment depthand gear type.     

Relationships among environment, spawning and settlement of Queen scallop in the Ría de Arosa (Galicia, NW Spain)

This study examines the relationship of the reproductive and reserve storage cycles and spat settlement of the Queen scallop (Aequipecten opercularis) to environmental factors. The possibility of farming this species from spat settled on collectors is considered. The gonad condition index shows maximum values between mid-May and early August. Another peak occurs in mid-November. In spring and summer, the energy needed for gametogenesis is derived from food, although it is possible that direct transfer may occur from the digestive gland to the gonad. The glycogen and lipid content of the reserve organs reaches maximum values between late summer and early autumn. The energy requirements related to gametogenesis, which begins in autumn, involve the consumption of accumulated reserves with the resulting reduction in the condition indices. There is a positive correlation between temperature and the condition indices of the digestive gland, the adductor muscle and their lipid and glycogen content, respectively. Two settlement periods were recorded, one in winter, which could not be associated with the spawning of the experimental animals, and another in summer, which coincided with the spawning that took place in spring. The reduced gonad indices recorded at the end of the summer and in winter did not lead to settlement.