Hatchery production of diploid and triploid clams, Tapes dorsatus (Lamarck 1818): a potential new species for aquaculture

To assess the potential for hatchery production of the venerid clam, Tapes dorsatus, diploid and triploid clams were produced and ongrown until the spat reached 5–8 mm in size. Triploidy percentages at metamorphosis that ranged from 56 to 85% were induced using a 15-min exposure to 1 mg/l cytochalasin B. No differences were observed in the growth rate of sibling diploid and triploid T. dorsatus larvae. Survival of diploid clams to pediveliger stage was however higher. Post-metamorphic growth and survival of diploid and triploid clams remained the same until the clams were removed from the hatchery to outdoor nurseries. Throughout the larval and early spat phases of production, T. dorsatus growth was similar to that reported for the Manila clam, Tapes philippinarum. Based upon its ease of culture, rapid growth and marketability, T. dorsatus are thought to have considerable aquaculture potential.     

蛤类寄生的鱼钩虫属形态学观察

采用活体观察和蛋白银染色法,对文蛤、青蛤、四角蛤蜊和菲律宾蛤仔寄生性鱼钩虫属内的种类进行了初步鉴定,并观察其基本形态学特征。从4种蛤中共鉴定出鱼钩虫属纤毛虫3种,即尖鱼钩虫、日本鱼钩虫和厚鱼钩虫,其主要形态学统计特征有一定差异,但不同种间都具有各自相对稳定的特征。日本鱼钩虫和厚鱼钩虫的感染率和感染强度均高于尖鱼钩虫,不同种鱼钩虫表现出较高的宿主专一性。     

胆碱受体化合物对厚壳贻贝幼虫变态的调控作用

为研究胆碱受体在厚壳贻贝幼虫变态发育过程中的作用,通过药理学手段调查胆碱类神经递质乙酰胆碱、氯甲酰胆碱及其拮抗剂六甲双铵和阿托品对厚壳贻贝幼虫变态发育调控作用。结果显示:在24 h暴露实验中,氯甲酰胆碱在10-5~10-4mol/L浓度表现出诱导活性,乙酰胆碱则无诱导活性。在持续暴露实验中,氯甲酰胆碱在10-5~10-4mol/L浓度表现出诱导活性,乙酰胆碱在10-6~10-4mol/L浓度表现出诱导活性。在拮抗剂实验中,在10-4mol/L氯甲酰胆碱或10-4mol/L乙酰胆碱存在时,N型胆碱受体拮抗剂六甲双铵对厚壳贻贝幼虫的变态均无抑制效果,表明N型胆碱受体可能并不在幼虫的变态发育过程发挥主导作用。M型胆碱受体拮抗剂阿托品在10-4mol/L氯甲酰胆碱存在时表现出抑制作用,且测试液中幼虫的变态率降为0%,表明M型胆碱受体可能参与调控厚壳贻贝幼虫变态发育过程。在整个药理学实验过程中无死亡幼虫出现,因而氯甲酰胆碱和乙酰胆碱可作为有效诱导物来促进厚壳贻贝幼虫的变态发育,尝试应用于该种的水产养殖过程;同时本研究为厚壳贻贝变态发育调控机制的研究提供有效理论依据。     

Establishment of shell growth analysis technique of juvenile Manila clam <Emphasis Type="Italic">Ruditapes philippinarum</Emphasis>: semidiurnal shell increment formation

ABSTRACT:   The conventional acetate peel method was modified to analyze the shell growth pattern of juvenile Manila clam Ruditapes philippinarum as small as 2 mm in shell length (SL). In the outer shell layer along the axis of maximum growth, two types of growth increments were observed: distinct increments and indistinct increments, which, respectively, do and do not continue to the middle shell layer. The distinct increments were found to be formed every two days in intertidal and shallow subtidal zones by field enclosure experiments of juveniles with datum points marked with alizarin complexone. Growth patterns of juveniles (12 mm SL) collected from the Seaside Park of Yokohama in Tokyo Bay were analyzed to confirm the modified method. Mean daily shell growth rate from April to July 2005 ranged 120–142 μm/day, which was reasonable as compared with previous studies. It was impossible to backcalculate the growth to the settlement size (i.e. 0.2 mm SL) because of erosion of the outer shell surface, and the smallest backcalculated minimum shell length was 0.8 mm. Fluctuations in daily growth rate were high, ranging 29–315 μm/day, and did not show a clear two-weekly rhythm.     

Effects of Temperature and Salinity upon Larval Growth, Survival and Development in Hatchery Reared Southern Atlantic Surfclams Spisula solidissima similis

Abstract.– Parameters associated with optimum larval-rearing conditions are important in developing the culturing protocol of potential aquacultural species, and have yet to be addressed in terms of water temperature and salinity for Spisula solidissima similis , the southern Atlantic surfclam. Hatchery spawned S. s. similis larvae were reared to late pediveliger stage in five simultaneously conducted water temperature and salinity treatments. This larval growth and survival experimentation consisted of three salinity treatments (15, 25 and 30 ppt) in conjunction with a water temperature of 20 C, and two water temperature treatments (15 and 25 C) in conjunction with a salinity of 25 ppt. In the 20 C temperature treatment, significantly higher larval survival and greater growth occurred (both, P < 0.0001) as compared to the 15 C and 25 C treatments by day 22. Complete larval mortality occurred in the 20 C, 15 ppt salinity treatment by day 4. No significant differences in larval survival occurred between the 25 ppt, 20 C and 30 ppt, 20 C treatments by day 22 (P = 0.714). However, significantly greater larval growth occurred in the 25 ppt, 20 C compared to the 30 ppt, 20 C treatment (P = 0.009). The optimum rearing temperature and salinity for hatchery spawned S s. similis larvae to late pediveliger stage are 20 C and 25 ppt, respectively, within the temperatures and salinities tested.     

Stocking density evaluation on Catarina scallop (Argopecten ventricosus,Sowerby II, 1842) larvae to improve hatchery production

The Catarina scallop Argopecten ventricosus is a highly valued resource. Although its hatchery spat production has already been reported, the effects of initial larval stocking density have never been reported for production purposes. This study evaluates A. ventricosus growth and survival in triplicate using three stocking densities: low (LD; 2 larvae mL^?1), medium (MD; 4 larvae mL^?1), and high (HD; 6 larvae mL^?1). Three-day old larvae were reared in 18-L plastic carboy at 25.6?±?0.5 °C and fed with a microalgal blend of Isochrysis galbana and Chaetoceros calcitrans (1:1 cell number ratio) for 7 days, equivalent to 10 post-fertilization days (PFD). Higher specific growth rate was recorded at LD (15.8?±?0.2%) after 8 PFD of culture compared to MD (1.6?±?0.5%) and HD (4.1?±?1.8%) densities. The least time required for 60% of the larvae to reach the pediveliger stage was recorded at LD condition (10 PFD). Higher survival was recorded at HD (58.8?±?3.1%) at 8 PFD compared to MD (53.5?±?3.1%) and LD (43.9?±?3.0%). After 8 PFD, stocking density was highly related to larval growth and survival. To increase production and growth, and reduce the time required to reach pediveliger stage, stocking density should start with 6 larvae mL^?1 and be reduced to 2 larvae mL^?1 at 7 PFD.

     

A herpes-like virus infecting Crassostrea gigas and Ruditapes philippinarum larvae in France

Concomitant sporadic high mortalities were reported in June 1997 among batches of larval Pacific oyster, Crassostrea gigas, and Manila clam, Ruditapes philippinarum , in a French commercial hatchery. Histological observation showed the presence of cellular abnormalities in affected animals. Electron transmission microscopy revealed the presence of herpes-like virus particles in infected larvae of both bivalve species. Viruses observed in C. gigas and R. philippinarum are closely related with respect to ultrastructure and morphogenesis. They were detected simultaneously in both bivalve species larvae indicating possible interspecific transmission. Moreover, PCR analysis using oyster herpes-like virus specific primers allowed amplification of fragments of expected sizes for both bivalve species and demonstrated the presence of viral DNA. The PCR products obtained for both bivalve species and digested by restriction enzymes displayed the same patterns. These data suggest that the same herpes-like virus may infect larval oysters and clams.     

Larval rearing of calico scallops, Argopecten gibbus, in a flow-through system

A flow-through (FT) culture system is described for calico scallop, Argopecten gibbus, larvae. Its performance was assessed by larval survival rate, shell growth, settlement rate and post-larval shell growth for the duration of larval life (13 days). Comparisons were made with larvae reared in standard static system (S). Effect of increased larval density on FT performance was also investigated. With comparable larval densities, survival rate of Day 2 larvae to pediveliger stage was similar in both larval rearing systems. Shell growth for FT-reared larvae was comparable or significantly higher than in the static system (P < 0.01). Settlement rate of pediveligers was comparable for both systems, averaging 30.7%, and no significant difference was seen in shell growth of FT- and static-reared pediveligers. Increased initial larval density did not affect survival rate in FT, but did negatively affect larval shell growth, settlement rate and post-larval shell growth yielding lower growth and minimal settlement rate (10.9 ± 2.8%) compared to the static system. This FT system was successful as larval rearing system, optimising space allocation in the hatchery, reducing labour, and eliminating the use of antibiotics. Optimising initial larval density within the system needs to be investigated in association with food ration.     

大竹蛏生产性人工繁育试验

2007年对大竹蛏进行了生产性人工繁育试验。对亲本不同批次催产效果、不同规格亲本产卵差异、孵化密度进行了比较,研究了D形幼虫发育与温度的关系以及幼虫发育各阶段生长规律等,结果显示,大竹蛏属分批成熟、分批产卵的潜居性贝类,不同批次个体平均产卵量(36~118)×104cell,个体总产卵量294×104cell。壳长8~10 cm的亲贝产卵量大,催产效果好。受精卵适宜的孵化密度为5~10 cell/mL。在水温21~24.5℃条件下,D形幼虫经8~5 d生长,发育变态为附着稚贝。D形幼虫壳长日生长33.33±4.22μm,1 mm前的稚贝壳长日生长108.33±22.57μm,1~10 mm的稚贝平均旬生长量2.12 mm,10.4~30.6 mm的苗种平均旬生长量为2.02 mm。当水温下降到15℃后,大竹蛏苗种生长滞缓。2007年培育出壳长11.52±0.27 mm的稚贝2 165×104cfu,平均成活率12.1%。     

Growth of pike larvae (Esox lucius) under different conditions of food quality and salinity

Abstract –  We measured growth of pike larvae ( Esox lucius ) fed with freshwater and brackish-water zooplankton by monitoring larval wet weight during 18 days. The fish food was analysed for species composition, carbon, nitrogen and fatty acids. Further, we analysed fish larval faecal pellet production. Larval weight was significantly higher in fresh water than in brackish water with natural zooplankton as food. Growth, given as wet weight, showed a significant relationship with zooplankton (>100  μ m) food carbon and highly unsaturated fatty acids, 20:5ω3, 22:6ω3, ω6 fatty acids and the ω3/ω6 fatty acid ratio. Phytoplankton fatty acids (10–50  μ m), such as polyunsaturated fatty acids, 20:5ω3, 22:6ω3 and the ω3 fatty acids also correlated strongly with the wet weight of pike larvae. We demonstrated that several factors impact on pike larval growth.     

Effect of different ions on larval metamorphosis of the mussel Mytilus galloprovincialis

Metamorphic responses of pediveliger larvae of Mytilus galloprovincialis to different ions were investigated through a series of bioassays. Effects of tetraethylammonium chloride (TEA) on inductive effects of these above ions were also investigated. Excess ions including Li⁺, Cs⁺, Rb⁺ and Ca²⁺ induced larval metamorphosis at 10^?3 M to 5 × 10^?2 M in 24‐h exposure assays. In continuous exposure assays, only excess Ca²⁺ showed inductive activity and induced 25% metamorphosis at 5 × 10^?2 M. Larval responses to Li⁺ and Rb⁺were inhibited by TEA, while induction of metamorphosis by Cs⁺and Ca²⁺ was independent of the presence of TEA. Thus, these ions used can be useful inducers of larval metamorphosis for application in the aquaculture industry. The finding provides new insights on the biochemical mechanism controlling larval metamorphosis in this species.     

Growth and Survival of Larval Red Sea Bream Pagrus major and Japanese Flounder Paralichthys olivaceus Fed Microbound Diets

To establish the practical use of microbound diets (MBD) for larval fish in mass seedling production, rearing experiments of larval red sea bream, Pagrus major , and Japanese flounder, Paralichthys olivaeeus , were conducted. A mixture of various protein sources was used, and dietary amino acid patterns were approximated to those of larval whole body protein. Two thousand red sea bream larvae and 1,000 Japanese flounder larvae, all 10 days old, were placed in 100 liter tanks with running sea water under ambient water temperature, which ranged from 18 to 20C. The particle size of MBD was 125 μm at the beginning of the experiment and adjusted as fish size increased thereafter. Employing MBD together with a small amount of live food could sustain the growth and survival of larval red sea bream and Japanese flounder. Thus, data from the present study indicates that substitution of artificial feeds for live foods is possible for larval fish production, although improvements in MBD diets may be necessary before they are adequate for large scale seedling production.     

Larval rearing and spat production of edible oyster Crassostrea gryphoides (Schlotheim)

The edible oyster Crassostrea gryphoides was induced to spawn in the laboratory by thermal stimulation, and the larvae were reared to spat. The larvae grow through the straight hinge (70×60.5 μm), early umbo (96.25×87.5 μm), late umbo (215×152.5 μm), eyed stage (290×222.5 μm) and pediveliger (308.25×254.17 μm) in pelagic phase before metamorphosing to spat, and these stages are described. These stages were reached at 20 h, on the fifth, 11th, 15th, 19th and 21st day respectively. Spat settlement percentage was found to be 1.8%.     

Embryonic development and influence of egg density on early veliger larvae and effects of dietary microalgae on growth of brown mussel Perna perna (L. 1758) larvae under laboratory conditions

The effect of egg density on embryonic development and larval quality as well as the lipid and fatty acid contents (eicosapentaenoic acid, EPA; docosahexaenoic acid, DHA) of cultured microalgae fed to Perna perna larvae was studied under controlled conditions to provide information needed for development of an experimental hatchery. Embryonic development followed the common sequence exhibited by other bivalves. d-larva stage was attained 40–44 h post-fertilisation at 21 ± 1 °C. The umbo-stage was reached in 11 days, and pediveliger larvae were observed 26 days post-fertilisation. Low egg density (range 20–100 eggs cm^?2) produced high proportions of normal d-larvae. Larval development showed two growth phases: 1st—the mixotrophic stage and 2nd—the exotrophic stage where the composition of diets had significant effects on larval growth with higher rates in larvae fed with the mixed microalgae (Isochrysis galbana + Chaetoceros calcitrans, I. galbana + Phaeodactylum tricornutum and I. galbana + Skeletonema costatum) in comparison with the monospecific diet (I. galbana). Fatty acid analysis showed that larval growth and survival were strongly influenced by proportions of dietary DHA and EPA. These results indicate that DHA and EPA are the key factors in determining larval performance, considerably more than the total amount of other fatty acids.     

Effect of temperature on survival,growth and development of Mytilus galloprovincialis larvae

Mussel aquaculture is widely prevalent worldwide, but generally relies on natural seed collection, which does not always meet the needs of the producers. Thus, development of mussel hatcheries is of economic interest in some parts of the world, such as Europe; it provides opportunities not only on annual reliability of seed but also on genetic improvements. To broaden knowledge on mussel larval physiology, we carried out temperature treatments (17, 20 and 24 °C) on Mytilus galloprovincialis larvae under laboratory conditions. The trials ended when 30% of the larval population was in the post‐larval stage. The temperature coefficient Q₁₀ indicated a strong relationship between temperature and increase in growth from 17 to 20 °C, but not between 20 and 24 °C. Exposure of M. galloprovincialis larvae to 17 °C resulted in poor growth, low survival and a delayed development and was considered to be inadequate for M. galloprovincialis larval culture. Rearing the larvae at 20 or 24 °C produced better growth, higher survival rates and faster metamorphosis as compared with 17 °C. The temperature region within 20 and 24 °C was suggested as adequate for the mussel M. galloprovincialis larval culture, and implications of these results on the development of commercial hatcheries were discussed.     

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.     

Optimizing stocking density and microalgae ration improves the growth potential of tropical black‐lip oyster,Saccostrea echinata,larvae

The combined effects of stocking density and microalgae ration on survival and size of Saccostrea echinata larvae were studied in two‐factor experiments for the major developmental stages: D‐veliger (1‐day posthatch [dph], Experiment 1), umbonate (12 dph, Experiment 2), and eyed (19 dph, Experiment 3) larvae. Larvae were stocked into replicate sets of four 10‐L aquaria with ambient 1‐μm filtered sea water (28 ± 1.5°C and 36 ppt) and cultured for four days at densities of 0.5, 2, 5, 7, or 10 larvae/mL and provided with microalgae rations at each of five densities (cells larvae^?1 day^?1); 0, 1, 3, 5, or 8 × 10³ (D‐veliger larvae, Experiment 1); 0, 5, 12, 18, or 25 × 10³ (umbonate larvae, Experiment 2); and 0, 15, 30, 40, or 60 × 10³ (eyed larvae, Experiment 3). Microalgae rations for each larval life stage were selected on the basis of increasing food requirement with larval size and comprised a 2:1:1 mixture of Chaetoceros calcitrans, Tisochrysis lutea, and Pavlova spp., calculated on an equal dry‐weight basis. Contour plots were generated from larval survival and larval size (dorso‐ventral measurement [DVM]) data to determine optimal culture conditions. Larvae showed high survival (54–100%) over a wide range of both treatment parameters across all life stages, confirming broad tolerance limits for this species. The interaction effects of larval stocking density and microalgae ration on larval size were significant (p < 0.001) across all life stages. Results indicate that maximum larval size (DVM) is achieved when S. echinata are cultured at: 6–8 larvae/mL and fed 5–6 × 10³ cells larvae^?1 day^?1 for D‐veligers (mean DVM >80 μm), at 2–8 larvae/mL and fed 11–25 × 10³ cells larvae^?1 day^?1 for umbonate larvae (mean DVM > 190 μm), and at 1–4 larvae/mL and fed 15–40 × 10³ cells larvae^?1 day^?1 for eyed larvae (mean DVM >230 μm). Results will help refine current hatchery methods for S. echinata supporting further development toward commercial aquaculture production of this species.     

Early life history of yellow puffer,Chonerhinos naritus (Richardson, 1848) from Sarawak,Northwestern Borneo

The growth and morphological development including fins, spine distribution and pigmentation of larval and juvenile of hatchery‐reared yellow puffer, Chonerhinos naritus were described to provide essential information on the early life history of this species. The total length (TL) of newly hatched larvae was 3.42 ± 0.23 (mean ± SD) mm, reaching 5.66 ± 0.38 mm on 5 days after hatched (DAH), 7.80 ± 0.28 mm on 11 DAH, 9.88 ± 0.40 mm on 27 DAH and 10.92 ± 0.58 mm on 30 DAH. The yolk was completely absorbed in preflexion larvae at 4 DAH. The mouth opening started at 3 DAH of yolk sac larvae, while the teeth appeared starting from preflexion larvae at 7 DAH. Overall aggregate fin ray numbers including caudal fin attained full complement in postflexion larvae at 27 DAH. Several melanophores with appearance of small stellate were first appeared dorsally on the head of flexion larvae at 13 DAH, expanded at the dorsal region of the head, above the eye in juveniles at 30 DAH. The spines first appeared in preflexion larvae of C. naritus at 7 DAH, covering the ventral skin region below pectoral fin base and expanded to the ventral part of the body and nearly covered the whole abdomen region before the anus and below the eyes in juveniles. C. naritus remain as larvae for approximately 29 days, during which they metamorphose to the juvenile stage prior to sexual maturation. Observations in larvae development of C. naritus revealed similar characteristics with other Tetraodontidae species.     

Biochemical changes during larval development in the short neck clam, Paphia malabarica Chemnitz

Biochemical compositions were determined for eggs, D-shaped larvae, umbo larvae and pediveliger of the short neck clam Paphia malabarica Chemnitz. Spawned eggs were composed of 63.2% protein, 25.4% lipid and 11.4% carbohydrate. After 48 h of embryogenesis, 2.6% of the protein, 11.8% of the lipid and 3.2% of carbohydrate mass had been lost, providing 20.5%, 75.4% and 4.1% of the total energy expenditure of 0.2147 mJ embryo⁻¹. During 48 h of metamorphosis, lipid was utilized first, followed by a heavy consumption of protein; protein, lipid and carbohydrate lost 23.8%, 50.2% and 32.5% of their mass respectively. Protein and lipid supplied a comparable amount of energy for metamorphosis, 34.2% and 55.2%, respectively, whereas, carbohydrate contributed only 10.6% to the 2.733 mJ larva^−l metamorphic energy expenditure.     

Use of premature New Zealand dredge oyster Tiostrea lutaria Hutton larvae for spat production

The New Zealand dredge oyster Tiostrea lutaria Hutton is an incubatory ostreid species that produces fully developed pediveliger larvae, which typically settle shortly after release from the parent. Broods of larvae obtained by opening incubating oysters provide a potential method of spat production, but only a small proportion of the broods obtained in this way are the late‐stage, ready‐to‐settle pediveligers. The majority of the broods are gastrula‐, trochophore‐ and veliger‐stage larvae. Experiments were undertaken to determine whether these early stages, as well as the pediveliger stage, could be reared through to settlement, and so make spat production based on opening incubating oysters much more efficient. Experiments conducted at three temperatures (ambient, ambient + 3 °C and ambient + 6 °C) and under three food regimes (with and without cultured microalgae and without dissolved organics) were unsuccessful in ex‐parent rearing of early larvae (gastrulae and trochophores). Later stage larvae, both veligers and pediveligers, were successfully reared, and high (> 75%) but variable levels of settlement were achieved. Ex‐parent rearing did not benefit from elevated temperatures or the presence of food, and settlement of spat from these prematurely released larvae may be reduced in the presence of food. The ability to rear veliger larvae, as well as pediveligers, greatly increases the potential to use the opening of incubating adult oysters during the breeding season as a source of dredge oyster spat.