Experimental deepwater culture of the Sydney rock oyster (Crassostrea commercialis): V. Commercial raft trials

Four large rafts (6.4 × 4.3 m), each costing $ A 543 totally equipped and holding 600 kg of trayed layers of oysters, were sited in New South Wales estuaries during 1977 and 1978. Small, single oysters (spat at 25–29 g whole weight or seconds at 29–40 g) were grown to restaurant (plate) grade (40–67 g).Sixteen crops were harvested, usually after three months growout. None showed evidence of overspatting (attachment of young oysters to the crop). Growth rates (measured as oyster weight increases) ranged from 5 to 30% per month and averaged 19%. In four of the crops mortality was high (12, 22, 22 and 90%) due to parasites, predators or wave action. In the remaining 12 crops natural mortality averaged 6% total for the growout period. The average actual wholesale value of the crops was $ A 422 and this could be raised to an estimated wholesale value of $A 527 per crop by utilising pregrowout grading and harvest date selection. Several husbandry practices are recommended. (1) Grading oysters mechanically before growout to produce more uniform crops. (2) Covering top trays to prevent fish attacks and losses through waves. (3) Deciding optimum harvest date by inspection after three months growth.     

Experimental deepwater culture of the Sydney rock oyster (Crassostrea commercialis = Saccostrea cucullata): II. Pontoon tray cultivation

Pontoons made from plastic pipe were tested as an alternative to racks for deepwater culture of the Sydney rock oyster. The growth and mortality of oysters permanently suspended in water on trays beneath floating pontoons were compared with oysters on trays in an intertidal zone. For both culled spat (30–31 g whole oyster weight) and seconds oysters (37–39 g) beneath pontoons the growth rate, measured by weight increases, was three times that of oysters on intertidal racks over a 5-month period. Mortality (from unknown causes) was higher beneath the pontoons. The mean mortality of spat oysters was 40% compared with 24% on the intertidal trays, and for seconds oysters was 51% compared with 34%.     

Commercial assessment of growth and mortality of fifth-generation Sydney rock oysters Saccostrea glomerata (Gould, 1850) selectively bred for faster growth

The Sydney rock oyster Saccostrea glomerata (Gould, 1850) industry acquired hatchery-produced spat selected for faster growth for the first time in January 2004. Selectively bred and non-selected (Control) spat produced concurrently were used to compare performance when grown under commercial conditions. Spat were distributed to farmers in seven estuaries in New South Wales. Individual farmers cultivated these oysters using their own techniques and growth and mortality were recorded quarterly. At each site, the two oyster types were cultivated using the same culture method, location and density. Growth was compared when oysters were 27 months of age. At this time, selectively bred oysters were significantly larger and heavier than Control oysters. The same result was obtained when oysters were compared at the point in time when selectively bred oysters had reached 50 g at each site. No significant difference was found for cumulative mortality between the selectively bred oysters and Control oysters across all sites. However, the seven sites had significantly different levels of cumulative mortality. Overall, the performance of selectively bred oysters was superior to the Control oysters and selectively bred oysters reached the 50 g bench mark within 29.3 months when averaged across all sites.     

Experimental deepwater culture of the Sydney rock oyster (Saccostrea commercialis). VI. Commercial oyster cage systems

A growout cage that retains oysters, excludes predators and reduces maintenance is described; it is cut from 200 mm (8 in) steel reinforcing mesh as kitset units and then hot dip galvanised. Each cage is 2.2 m long, 0.8 m wide and 1.0 m deep (88 × 22 × 40 in) and contains five floors which are 203 mm (8 in) apart. The floors and the walls are covered with 19 mm ($\text{3}\text{4}$ in) galvanised wire mesh, or high density polyethylene plastic mesh. These cages may be slung from rafts, fitted with individual flotation or lowered to the bottom with a marker buoy; they weigh approximately 70 kg (154 lb) empty and about 220 kg (484 lb) when harvested. Each cage crop consists of approximately 2.5 bags totalling about 150 kg (330 lb), and in good growing areas three to four crops have been harvested from each cage per year. In two such crops culled spat (22–29 g whole wet weight) were converted to plate (first grade) oysters (40–67 g); in the other two, seconds (29–40 g) were converted to plate oysters. Growth rates, stocking densities and mortality data are given for 11 crops.     

Culture of the American oyster, Crassostrea virginica (Gmelin 1971) in Rio Lagartos, Yucatán, México

This research was done with the purpose to ascertain the biological feasibility of the culture of Crassostrea virginica (Gmelin 1971) at Rio Lagartos lagoon in Yucatán, México. Spat from two localities of the Golfo de México were grown in Nestier boxes: spat from Tamiahua, Veracruz, which had an initial average height of 22.50 ± 5.10 (SD) mm and initial total wet weight of 2.90 ± 1.64 g and spat from Mecoacán, Tabasco, that were 32.05 ± 4.50 mm and 5.53 ± 0.03 g, respectively. Both groups of oysters reached commercial size after 10 months of culture. Veracruz spat reached 65.00 ± 6.80 mm in height and 33.26 ± 7.02 g in total wet weight. Those from Tabasco reached 62.90 ± 6.70 mm in height and 33.97 ± 9.95 g in total wet weight. The mean physiological condition index for oysters from Tabasco was 5.96% and from Veracruz was 4.52%. Total survival rate was 63% for spat from Veracruz and 55% from Tabasco. Environmental conditions in the culture area proved to be favourable for the rearing of C. virginica.     

Growth of the European flat oyster in the Mediterranean Sea (Murcia, SE Spain)

Growth of the natural European flat oyster (Ostrea edulis L.) spat from the Mar Menor (Murcia, Spain) was studied in the Mediterranean Sea over 18 months. The oysters were cultured in two types of containers, stackable plastic Galician trays and plastic mesh pots, deployed at a depth of 15 m hung from a long-line. Two size classes of spat were used, Class I spat (initially 53 mm in size and 19 g in weight) and class II spat (initially 31 mm, 4 g). The best results were observed in the class I oysters grown in the trays, which yielded a substantial biomass (24.77 kg m^–2), the survival rate was 69% and commercial size (60 mm) was attained by all the oysters within 9 months of the start of the experiment. The observed growth of the class II oysters was poor, attaining a mean of not more than 50 mm and 18 g; the survival rate ranged between 25–74% and only between 8–13% of the class II spat attained commercial size.     

The effect of mesh covers on the survival and growth of Crassostrea gigas Thunberg grown on the sea bed

Growth and mortality were measured in samples of Crassostrea gigas planted in trays on the beach at 4.5, 7.5 and 20% exposure. The oysters were graded by live weight into < 1, 1 2, 3–4, 5 6 and 8–10-g groups at planting. Three levels of protection were provided: none, 36-mm and 12.5-mm mesh. Five separate trials of 41–108 days covered about a year.Mortality decreased with increasing size of oyster at planting and with increasing degree of cover. On average, oysters of < 1 g and without cover showed 50% survival over 30 days, while oysters of 3–4 g protected with a 12.5-mm mesh showed 97% survival. Neither seasonal variation in survival nor variation related to exposure was detected. Unprotected oysters grew to a smaller size than protected oysters and those at 20% exposure grew less than those at 7.5 or 4.5% exposure. It is probable that the two sizes of mesh provided protection against interference and predation by the shore crab Carcinus maenas.The combined results of the trials indicated that the standing stock at the end of about 6 months, which included the summer, obtained from laying 100, 0.6 g oysters at 4.5% exposure would be 564 g and 99 g with 12.5-mm mesh and no protection, respectively.     

Reproductive condition of the pearl oyster, Pinctada imbricata, Röding, in Port Stephens, New South Wales, Australia

In an investigation of the potential for pearl production in New South Wales (NSW), Australia, changes in the physical and reproductive condition of the pearl oyster, Pinctada imbricata, were monitored for over 2 years. Using wild oysters gathered from close to the southern extent of the species' range in Port Stephens, NSW, a series of macroscopic and histological observations were made. Reproductive activity in P. imbricata was greatest from late spring to early autumn with oysters in poor reproductive condition during winter. Peaks in reproductive indices occurred in November 1998, March 1999, December 1999 and April 2000. Four indices of physiological condition were used: shell growth, byssal attachment, mantle thickness and mucoprotien layer. With the exception of the thickness and extent of the mucoprotein layer, these indices either showed little variation or the variation that occurred was not related to seasonal or reproductive changes. Changes in the mucoprotein layer were correlated with water temperature and suggest that this layer is metabolized during periods of high demand such as during gonadogenesis. Collectors deployed at two sites in Port Stephens demonstrated that spatfall occurs largely in the months of December and January following the spring and early summer peaks in reproductive activity (November 1998 and December 1999). Spatfall was not observed following the autumnal peaks (March 1999 and April 2000) in reproductive activity. Overall, reproductive patterns in P. imbricata are poorly suited to spat supply in Port Stephens. Farmers require spat in early spring (September) to allow maximum use of the ‘growing’ season (September–May). Reproductively capable oysters are not available from the wild until September and quantity of natural spatfall is too variable and occurs too late in the season (December–January). As a result, oysters are being conditioned in the hatchery in July, spawned in August and spat are supplied to farmers in mid September.     

The effect of food quality on glycogen content,the fatty acid profile and winter mortality in cultivated oyster spat (Ostrea edulis)

Winter mortality in hatchery reared oyster spat (Ostrea edulis) that received three different diets during the summer period was investigated. Oysters fed a natural type diet had a winter mortality of 18.3 ± 6.3% while oysters fed cultivated algae (a mixture of Tetraselmis suecica, Isochrysis galbana and Chaetoceros muelleri) had a mortality of 73.0 ± 9.7%. A group of oysters fed a mix between the two diets had a mortality of 54.7 ± 10.6%. Tissue samples were taken at the start of the experiment, after the summer period and after the winter period in order to determine growth and the content of glycogen and fatty acids. The glycogen content decreased for all groups during the winter but the decrease was highest in oysters fed the natural diet. This group also contained the largest variety of fatty acids, but there was no difference in the content of the essential fatty acids EPA, DPA and DHA between the groups. It is concluded that transplantation of spat to the sea in spring and early summer may reduce winter mortality since the feeding period on a more varied natural algal diet is prolonged compared to transplantation of spat later in the season.     

Experimental deepwater culture of the Sydney rock oyster (Crassostrea commercialis=Saccostrea cucullata): I. Growth of vertical clumps of oysters (‘ren’)

Japanese style ren, consisting of scallop shells encrusted with small Sydney rock oysters and strung on vertical wires, were grown at 23 estuarine stations along the New South Wales coast for up to 21 months. Weight increments of ren were used to evaluate growth rates of oysters in non-cumulative (3–4 months immersion) and cumulative (6–21 months immersion) series. Oyster weight increased at a rate of approximately 10% per month, which was considered suitable for commercial production, but estimated labour costs to make up the ren were high. Mortality rate was 6.3% per 3–4 months immersion. Gaping oysters, through natural mortality, winter mortality, the haplosporidian parasite Marteilia sydneyi, and other causes, accounted for 4.5%. Broken oysters, resulting from fish and crab predation, accounted for 1.8%. Mortality caused by the polychaete mudworm Polydora websteri was negligible; only 1.7% of the 4.5% gapers showed the characteristic blisters.     

Experimental deepwater culture of the Sydney rock oyster (Crassostrea commercialis): III. Raft cultivation of trayed oysters

Sydney rock oysters, normally intertidal, were submerged below rafts in vertical stacks of 15 oyster trays extending 2 m deep. Growth rates and mortality were not good or economically encouraging. The best growth was from small culled spat (43 whole oysters/kg) to large seconds (28/kg), an increase of 59% in 9 months. The minimum mortality was 52%. Fouling growths of barnacles, tunicates, sponges and hydroids were restricted by placing experimental trays on top of the raft for several days to dry out. Compared with controls, this resulted in increased oyster growth in experimental trays during the next 6 months. Oyster mortality and incidence of mudworm blisters (resulting from the polychaete Polydora websteri) were similar in both control and experimental trays during this period. For improved growth of trayed submerged oysters the optimum vertical distance between trays and the optimum density of oysters on trays need to be determined.     

Mortality associated with OsHV-1 in spat Crassostrea gigas: role of wild-caught spat in the horizontal transmission of the disease

The French oyster production of Crassostrea gigas is based on two sources of spat: wild-caught (WC) and hatchery-produced (HP). Massive mortality related to the ostreid herpesvirus type 1 (OsHV-1) has affected both sources in France since 2008. We investigated the mortality in juvenile C. gigas due to the horizontal transmission of OsHV-1 within (separated condition) and between (mixed condition) the two spat sources in three environments from April to June 2010. In the separated condition, no mortality was observed in the HP batches, while the WC batches experienced moderate to high mortality (40–80 %). In contrast, the WC and HP batches experienced high mortality in all tested environments for the mixed condition. At the beginning of the trial, the HP batches were all negative for OsHV-1 DNA detection by real-time PCR, while the WC batches were all positive for OsHV-1 DNA detection by real-time PCR, even though the percentage of virus DNA-positive oysters and viral load were low. During the experiment, all batches that exhibited mortality were positive for OsHV-1 with a high viral load, while OsHV-1 was never detected for the HP batches of the separated condition. Together, our results demonstrated that OsHV-1 was horizontally transmitted from the WC oysters to the HP oysters. Our study is the first to indicate that the mortality related to OsHV-1 in HP oysters can be avoided using ponds or tanks. However, these oysters were always protected from OsHV-1, and HP oysters could also experience mortality and spread the disease similar to the WC oysters if such care is not used. Finally, the persistence of OsHV-1 at a sub-clinical level in certain oysters supports the hypothesis that the virus can be reactivated and cause viral replication. The use of the two spat sources is discussed to better understand the spread of the disease among oyster stocks.     

Gametogenetic cycle and reproductive effort assessed by two methods in 3 age classes of Pacific oysters, Crassostrea gigas, reared in Normandy

Two methods were used to estimate the reproductive output of female Pacific oysters reared in Normandy: histology with image analysis and ELISA (Enzyme-Linked ImmunoSorbent Assay) which allowed the quantification of egg protein. Condition indices, gonad area and gametogenetic stages of the oysters were determined in the entire population (males and females) between May and October 2005. All investigations were performed in 3 age classes: oysters in their first, second or third years (corresponding to spat, half-grown and market-sized oysters, respectively). Both quantitative histology and ELISA provided similar results in terms of reproductive effort (illustrated by the gonado-somatic index, GSI) except during the GSI drop, corresponding to spawning, which was less marked with the ELISA method. Growth depended on oyster age, the sex ratio was well balanced and the reproductive cycle was synchronized in all age classes. In the 3 age classes, most of the oysters were ripe and ready to spawn on August 8, and ten days after the post-spawning stage was observed in 40% of spat oysters and 70% of half-grown and market-sized bivalves. The major difference between age classes was observed in the reproductive investment, with spat having a lower reproductive output. For example, in males and females, the gonad area reached 78–79% in the median animal section at full maturity (August 8) in half-grown and marketable oysters while it attained only 59% in spat. At the same time, GSI in females was, respectively in spat and the 2 oldest age classes, 33% (quantitative histology)–36% (ELISA) and 55% (quantitative histology)–60% (ELISA). The mean assessed gonad weight and fecundities increased with the age of the oysters: 1.3 g and 12 million eggs, 7.8 g and 135 million eggs, and 11.5 g and 146 million eggs in spat, half-grown and market-sized oysters, respectively. Marked differences thus appear between 2 and 3-year-old oysters and spat. As early as their first reproductive cycle, the young oysters not only showed the reproductive features of the species in Normandy, but also a pronounced lower reproductive effort. This lower energy demand could explain their higher survival rate.     

Nursery growth, survival and chemical composition of great scallop Pecten maximus (L.) spat from different larval settlement groups

Scallop Pecten maximus spat (1.3–2.1 mm shell height) from different settlement groups were transferred from hatchery to land‐based nursery at different ages and sizes. Chemical content, growth and survival were compared at transfer time and after 1 and 8 weeks of nursery growth. Growth was lowest and mortality highest in the first week after transfer. Mean shell height growth was 21.5–71.4 μm day^?1 and ash‐free dry weight (AFDW) growth ?2.7 to 10.3 μg day^?1. Spat from the first settlement group attained a larger size and weight than spat from larvae settled 3 days later, but had a lower daily growth rate (%). Keeping the late‐settled spat a longer time in the hatchery to reach a bigger size before transfer seemed not to improve subsequent nursery growth. Survival showed a large variation with mean survival ranging from 32% to 74%. A substantial reduction in lipid content was found after transfer to the nursery. Sterol content at transfer was the only lipid class correlating with survival in the nursery. Based on the results, it is justified that spat groups of different settlement age are included in production of 15‐mm great scallop spat if they are transferred from the hatchery at the same age.     

Development and distribution of the non-indigenous Pacific oyster (<Emphasis Type="Italic">Crassostrea gigas</Emphasis>) in the Dutch Wadden Sea

Pacific oysters (Crassostrea gigas) were first observed in the Dutch Wadden Sea near Texel in 1983. The population increased slowly in the beginning but grew exponentially from the mid-1990s onwards, although now some stabilisation seems to be occurring. They occur on a variety of substrates such as mussel beds (Mytilus edulis), shell banks, dikes and poles. After initial settlement spat may fall on older individuals and congregate to dense clumps and subsequently form reefs. Individual Pacific oysters grow 3–4 cm long in their first year and 2–3 cm in their second year. Many mussel beds (Mytilus edulis) are slowly taken over by Pacific oysters, but there are also several reports of mussel spat settling on Pacific oyster reefs. This might in the end result in combined reefs. Successful Pacific oyster spat fall seems to be related to high summer temperatures, but also after mild summers much spat can be found on old (Pacific oyster) shells. Predation is of limited importance. Mortality factors are unknown, but every now and then unexplained mass mortality occurs. The gradual spread of the Pacific oyster in the Dutch Wadden Sea is documented in the first instance based on historical and anecdotal information. At the start of the more in-depth investigation in 2002, Pacific oysters of all size classes were already present near Texel. Near Ameland the development could be followed from the first observed settlement. On dense reefs each square metre may contain more than 500 adult Pacific oysters, weighing more than 100 kg per m2 fresh weight.     

Effects of temperature and photoperiod on the conditioning of the flat oyster (Ostrea edulis L.) in autumn

The production of the flat oyster Ostrea edulis (L.) natural spat in Europe has decreased almost by 60% in the past ten years. Thus, the importance of the production of oyster spat in hatcheries is evident. One of the critical steps in hatchery production is broodstock conditioning, especially difficult in autumn, when gonadal development is in resting period. Conditioning is influence by temperature, photoperiod and nutrition. In this work, the effects of two temperature and three photoperiod regimes on the conditioning of O. edulis were studied for three years by stereological analyses and registering number and dates of spawning and larval yield. Temperature had a positive effect on the gonadal development of O. edulis during conditioning. The percentages of germinal cells in oysters conditioned with a gradient of temperature (14–18°C) were double compared to oysters conditioned at 15°C. Oysters conditioned with longer photoperiods showed higher percentages of germinal cells. There was no interaction between temperature and photoperiod. Spawning was observed in the oysters treated with daylight (8–16 h) ten weeks from the beginning of conditioning. Flat oysters conditioned with 8 h and 8–12 h of daylight delayed the first spawning for a month. Total larval production was higher in the oysters treated with the longest daylight gradient. Gonadal and gametogenic development was a non‐synchronic process and the spawning extended for around two months. A protocol for flat oyster broodstock conditioning in autumn by using both a gradient of temperature (14–18°C) and daylight (8–16 h) is proposed.     

Early growth and reproduction of hatchery-produced Pacific oyster Crassostrea gigas in Gamakman Bay off the southern coast of Korea

We investigated the early growth and reproduction of hatchery-produced Pacific oysters Crassostrea gigas raised in a suspended long-line facility in Gamakman Bay, off the south coast of Korea. In October 2009, 4?months after transplanting, shell length had increased from 27.4 (July) to 82.5?mm (October), and tissue weight had increased from 0.2 to 5.2?g, indicating that the oyster had reached a marketable size in this month. Histological studies indicated rapid gonad maturation, and the oysters spawned during August and October, with a peak in September. An enzyme-linked immunosorbent assay used to quantify egg biomass revealed that the oysters produced a relatively small quantity of eggs, ranging from 5.1?% (August) to 8.8?% (September) of their body weight. The low total carbohydrate reserve in the tissue recorded in August and September coincided with intense energy utilization due to spawning, while the protein maximum in September matched peak egg mass. Our results suggest that hatchery-produced seed could supply a portion of the spat required in Gamakman Bay as well as in other oyster culture grounds of Korea, where the oyster industry is facing a shortage in the supply of natural spat.     

Growth,mortality and reproductive traits of diploid and triploid Pacific oysters (Crassostrea gigas,THUNBERG, 1793) in Southern Brazil

This work aimed to evaluate the whole weight (g), shell height (mm), mortality (%) and reproductive aspects (condition index and histology) of triploid (3N) Pacific oysters (Crassostrea gigas) cultivated in southern Brazil. To accomplish this, a comparative experiment was performed with a diploid (2N) control group in two cultivation sites on Santa Catarina Island: North Bay (NB) and South Bay (SB). Whole weight, height and cumulative mortality were evaluated monthly for eight months and condition index (CI) for six months. Histological analysis was performed every two weeks for four months to investigate reproductive aspects. At the end of the experiment, whole weight and height were similar for 3N and 2N oysters. However, while more growth in whole weight and height was observed in the initial phase of cultivation in NB, such growth was not detected in SB until intermediate and final grow‐out phase. At harvest, cumulative mortality in 3N oysters was similar that in 2N oysters. The results suggest that diploid and triploid oysters grown in southern Brazil have similar developmental patterns based on whole weight and height, as well as reproductive cycle. In addition, cultivation sites have more influence on growth and mortality than ploidy levels.     

Growth of the oyster Crassostrea corteziensis (Hertlein, 1951) in Sonora, Mexico

This is the first evaluation of growth and survival of spat of the Cortez oyster Crassostrea corteziensis (Hertlein) produced under controlled conditions in a coastal area in the state of Sonora, Mexico for aquaculture purposes. A suspended culture technique, used for the Pacific oyster C. gigas, was used. The Cortez oyster has an isometric shell growth during the first 13 months, reaching 71.3±1.9 mm length, 52.6±1.3 mm thickness and 25.1±0.8 mm width. Allometric growth was found between total weight and length, thickness and width (survival was 70%). The relationships between particulate organic, inorganic material, chlorophyll a and environmental parameters with growth are described. Growth rates of C. corteziensis were affected by temperature with retardation at less than 18°C. For aquaculture purposes, it is recommended that spat be sowed after winter, and oyster harvest occur at the end of autumn. According to the von Bertalanffy equation, Cortez oysters would reach the traditional exploitation size of 65 mm (mean length) at harvest. Finally, the results of this study have shown that C. corteziensis is a good candidate for aquaculture projects in this region.     

The growth and survival of experimental batches of hatchery-reared spat of Ostrea edulis L. and Crassostrea gigas thunberg,using different methods of tray cultivation

The seasonal growth and survival of experimental batches of hatchery-reared spat of the European oyster (Ostrea edulis) and the Pacific oyster (Crassostrea gigas) was followed in North Wales during the period 1972 to 1975. Three methods of tray cultivation were compared. These were: (a) trays suspended from a raft in the Menai Straits, (b) trays supported on trestles on the foreshore of the Menai Straits, and (c) trays in a laboratory nursery system which were supplied with sea water from Conwy estuary via a pumped storage system.Growth of oysters in the nursery system was consistently inferior to that of oysters kept at either site in the sea. Although in several years there were significant differences between the growth of oysters on the raft and in trays supported by trestles, on average neither site consistently produced larger oysters.Survival was significantly better in the nursery system for both species of oyster, but no consistent differences in survival were observed between either site in the sea.Seasonal growth of both species of oyster as well as the mortality of O. edulis were positively related to temperature. It was concluded on the basis of cost that (i) cultivation in systems employing pumped sea water would not be viable in the long term, and (ii) raft cultivation would only be suitable for post-hatchery sized oysters up to about 5 g live weight.