Dietary impact of algal and artificial diets, fed at different feeding rations, on the growth and fatty acid composition of Tapes philippinarum (L.) spat

The effect of lipid supplementation and algal ration on growth and fatty acid composition of juvenile clams, Tapes philippinarum was investigated. A diet of Tetraselmis suecica was supplemented with a lipid emulsion and fed at a daily ration of 0.5, 1.0 and 1.5% WW DW⁻¹ day⁻¹. A mixed algal diet of Isochrysis galbana (clone T-Iso) and T. suecica (1:1 on DW basis) and starvation functioned as positive and negative control treatments, respectively. T. suecica, which contains eicosapentaenoic acid (20:5n−3) but no docosahexaenoic acid (22:6n−3), was supplemented with 50% (% of algal dry weight) of a 22:6n−3-rich emulsion. Higher growth rates of T. philippinarum were associated with higher T. suecica feeding rations. Lipid supplementation resulted in significantly better growth rates of T. philippinarum at a T. suecica ration of 0.5, 1.0 and 1.5% WW DW⁻¹ day⁻¹. The growth promoting effect of lipid supplementation was significantly reduced during 4 consecutive weeks or by increasing the algal feeding ration. Increasing T. suecica rations were associated with a decrease in the % composition of 22:6n−3 while the 20:5n−3% composition was hardly affected in the total lipids of T. philippinarum. On the contrary, the absolute concentration of 22:6n−3 (μg per gram dry weight, μg g DW⁻¹) in the total lipids of T. philippinarum was similar at all T. suecica rations while the 20:5n−3 concentration significantly increased. The major effect of lipid supplementation on the fatty acid composition of the clams, was a significant increase of the 22:6n−3% composition in the total lipids, polar lipids and triglycerides. In contrast with 20:5n−3, the effect of lipid supplementation on the absolute 22:6n−3 content (μg g DW⁻¹) was more pronounced at a higher T. suecica ration. After a starvation period of 4 weeks, the concentration (μg g DW⁻¹) of all fatty acids was significantly reduced, except the n−7 monoenoic fatty acids (MUFA) and the non-methylene interrupted dienoic fatty acids (NMID). The concentration (μg g DW⁻¹) of the NMID in starved clams and clams fed different diets was similar to the concentration in the initial sample. This indicated that growing spat was actively synthesising NMID and they were selectively retained in unfed animals. The results indicated that either dietary lipid or 22:6n−3 was a growth-limiting factor when T. suecica was fed at a ration of 0.5, 1 and 1.5% WW DW⁻¹ day⁻¹. A selective retention in starved clams and a preferential accumulation in fed clams was observed for 22:6n−3 but not for 20:5n−3 which indicated a greater importance of 22:6n−3 compared to 20:5n−3.     

Gametogenic cycle and variations in oocyte size of Tapes philippinarum from the Lagoon of Venice

The gametogenic cycle of the clam Tapes philippinarum was studied in two populations from different areas of the Lagoon of Venice: S. Angelo (central basin) and Chioggia (southern basin). Samples were collected at regular intervals from July 2000 to July 2001. The study was performed by microscopic observations of histological sections of gonadic tissue and by measuring follicular and oocyte sizes by image analysis. Gametogenesis began in January and was clearly evident until May. Ripe clams appeared in April, and most active spawning occurred in May, continuing during summer until September. Measurements performed using image analysis (i.e., follicular area, percentage of reproductive tissue, oocyte diameter, percentage of resorbing area) highlighted environmental differences between the two sampling sites, demonstrating the better condition of clams from Chioggia.     

Larval and post‐larval growth,spat production and off‐bottom cultivation of the smooth venus clam Chionista fluctifraga

Harvesting practices of the clam Chionista fluctifraga show a decline in commercial size and densities, but no strategies have been developed to maintain clam beds. Aquaculture represents an alternative for preserving this resource. Adult clams from commercial grounds were used as broodstock. Conditioning, induction of spawning, cultivation of larvae, settlement of eyed larvae and nursing of postlarvae were performed in the hatchery for producing spat. Larvae and postlarvae were used to measure increase in shell height and data were fitted to exponential growth models. Spat were placed in floating trays and maintained in off‐bottom cultivation for 9 months. Samples of clams and tissues were collected monthly to measure absolute growth, shell height increase and a condition index. Larvae, postlarvae and juveniles showed exponential growth patterns. Mean shell height increased about 0.030 mm day^?1 during larval and post‐larval stages and 0.049 mm day^?1 during field cultivation. Pediveligers (height 215 ± 83 μm) entered metamorphosis at days 9–13 after fertilization, and postlarvae reached 3011.7 ± 325.5 μm (height) at day 60. After field cultivation, survival was about 95%; juvenile shell height was 20.6 ± 2.2 mm, and total weight was 5.3 ± 0.7 g. Growth rates were superior to natural conditions and the condition index was high throughout the study. Our results show that spat of C. fluctifraga can be produced in the hatchery, and that field production can be maintained in off‐bottom trays until reaching commercial size. Aquaculture activities for this species need to be established and evaluated.     

Farming triploid oysters

Although the commercial benefits of triploidy have been evaluated in the Pacific oyster Crassostrea gigas (Thunberg, 1793), eastern oyster C. virginica (Gmelin, 1791), Sydney rock oyster Saccostrea glomerata (Gould, 1850) and European flat oyster Ostrea edulis (Linnaeus, 1750), so far this technique has only been commercialised for Pacific oysters.

Commercial production of triploids on the West Coast of North America began in 1985. Since then production of triploids has greatly increased and the use of tetraploid males to fertilise eggs from diploids to produce batches of 100% triploids has been developed. In 1999/2000, triploid Pacific oysters made up 30% of all Pacific oysters farmed on the West Coast of North America. Some hatcheries now use tetraploid males instead of chemical or physical stress to produce triploids. The rapid uptake of triploid and tetraploidy techniques has been facilitated by the almost total dependence that these oyster industries have on hatcheries for the supply of seed. This industry in the Pacific Northwest of the US and in British Columbia, Canada, would not have developed to its current size without hatchery seed supplies. Triploids are preferred over diploids in summer because diploids are less marketable when in spawning condition.

There was only limited interest in triploidy production in France until 1999, when IFREMER began to make sperm from tetraploids available to commercial hatcheries. In 1999/2000, only 10% to 20% of all the hatchery-supplied Pacific oyster spat were triploids, but with the use of sperm from tetraploid oysters, this could increase sharply.

Elsewhere around the world, the commercial uptake of triploid oysters has been slow to develop. However, in countries where the production of Pacific oysters is based on hatchery supply of seed, it is likely that with the use of tetraploid oysters, the farming of triploid oysters will increase in the near future.     

The breeding potential and biochemical composition of triploid Manila clams, Tapes philippinarum Adams and Reeve

In 1989 and 1990. triploid Manila clam, Tapes philippinarum Adams and Reeve, seed were reared to 15-20 mm at the Fisheries Laboratory, Conwy, and planted out in the Menai Strait, North Wales. In each of the summers of 1992 and 1993, three of these batches, at 2, 3 or 4 years old, were returned to the laboratory to assess ploidy, size, spawning potential and biochemical composition. Percentage triploidy at this time was similar to that in the seed. After 6 and 8 weeks of warmwater conditioning. Only 45 out of l21 triploids (37%) were induced to spawn by thermal shock, with only one spawning as a male. By comparison, 75% of diploid clams spawned with a 1:1 ratio of males to females. Mean fecundity of triploids was significantly lower than that for diploids, at 0.497 compared with 1.54 million eggs per female. Compared with eggs from diploid females, eggs from triploids were larger and significantly fewer of them developed into D-larvae when fertilized by sperm from diploid males. Triploid clams were heavier and had a higher condition index and carbohydrate content than diploids of the same age, but lipid levels were similar. Potential advantages of producing and cultivating 100% triploid batches of Manila clam seed are discussed.     

Adding value to live, commercial size soft-shell clams (Mya arenaria L.) in Maine, USA: results from repeated, small-scale, field impoundment trials

The soft-shell clam (Mya arenaria L.) fishery in the state of Maine, USA, is worth $5–10 million annually and is primarily based on the sale of live individuals. More than 80% of the catch is sold for the “steamer clam” market that is highly seasonal due to supply and demand. Prices paid to harvesters for live clams throughout the year increases by as much as 70% during a 4-month period between early spring and late summer. If clams harvested in the spring could be held until late summer, a value-added product could be developed in this fishery. From April to August 1996, at an intertidal and subtidal location in eastern Maine, I tested whether it was biologically feasible to impound commercially harvested clams (shell LENGTH=44–75 mm) at densities between 720 and 850/m² using cages and nets (1.12 m²) to protect animals from predators. Survival was 91.7% (n=12) and 91.6% (n=6) at the intertidal and subtidal site, respectively. There was no discernible shell growth during this period and there was no difference between initial and final clam weights. The methodology was transferred to commercial harvesters in two Maine communities: Wiscasset (1997 and 1998) and Perry (2000). Impounded clams ( =21.8 kg/cage; n=18) lost, on average, 5 kg/cage in 1997 and 1998, whereas no significant net loss in wet weight occurred in cages deployed in 2000 ( =23.2 kg/cage; n=3). Differing harvesting and handling methods of individual clammers, prior to impounding clams, likely explains the variation in weight lost during the impounding periods. The difference in price per live kilogram between the beginning of the impounding period and the August sale date resulted in an average gain of $13.60/cage for clammers in 1997 and 1998 and $57.73/cage in 2000. Simple culture techniques can be used to increase the value of the live harvest of soft-shell clams along the coast of Maine. Clam impoundments may be a way for communities that co-manage the public clam resource with the state's marine resource agency to generate funds to pay for traditional management schemes, as well as enhancement programs that employ hatchery-reared juveniles. In addition, an indirect benefit of clam impoundments might be to create spawner sanctuaries since animals are impounded during the time when gamete release occurs.     

Preliminary studies on a chlamydial agent in the digestive diverticular epithelium of hard clams Mercenaria mercenaria (L.) from Great South Bay, New York

Abstract. The prevalence of a chlamydial infection in hatchery-reared adult hard clams Mercenaria mercenaria (L.) from Great South Bay, Long Island, New York was relatively high and seasonally stable. Infection occurred early in life while juvenile clams were still within the hatchery. Fluorescent antibody tests suggested that the clam agent shares the group antigen specific for chlamydia, but to a lesser degree than a known chlamydial strain used as a positive control. The method of Gimenez failed to stain elementary bodies in clam cell inclusion bodies. Based on the observations of this study, the inclusion body agent in the hard clam differs from known strains of chlamydia. Characterization of the clam chlamydia must await the successful propagation of the agent.     

When should pearl oyster,Pinctada margaritifera (L.), spat be transferred from the hatchery to the ocean?

Hatchery propagation of pearl oysters is relatively new and optimal hatchery protocols are still being developed. While in the hatchery, pearl oyster spat are supplied a constant and reliable food source and are protected from fluctuations in environmental conditions and predators. This study investigated the hypothesis that retaining blacklip pearl oyster, Pinctada margaritifera (L.), spat in the hatchery for longer periods, prior to transfer to the ocean, would improve growth and survival during early nursery culture. Results showed that the longer spat were retained in the hatchery, the smaller their average size at grading (3.5 months of age). At grading, spat transferred 3 weeks after settlement had a mean dorso–ventral shell height (DVH) of 9.2 ± 0.4 mm with 34% of individuals retained on a 10‐mm mesh. However, spat retained in the hatchery until 5, 7 and 9 weeks after settlement, had a mean DVH of 9.0 ± 0.4, 7.8 ± 0.3 and 6.3 ± 0.4 mm respectively. Only 10% of spat transferred 9 weeks after settlement were retained on a 10‐mm mesh at grading. The results probably reflect superior nutrition available in the ocean and indicate that pearl oyster spat should be transferred from the hatchery as soon as possible after settlement in order to maximize growth.     

Comparison of Three Culture Methods for the Intensive Culture of Northern Quahog Seed, Mercenaria mercenaria

A number of approaches have been utilized for growing bivalve hatchery seed (1 mm) to a size suitable for field planting (< 8 mm) but few have been directly compared. This study evaluated the growth and survival of northern quahog seed in three different culture systems and two different stocking densities. The three systems were: 1) a stacked-tray unit with downward water flow; 2) traditional upweller culture units with water flowing upward without seed bed expansion; and 3) upweller culture units with water flowing upward at fluidization velocities to provide seed bed expansion. The two stocking densities were 1.0 and 3.0 g whole wet weight clam/cm² respectively. During each trial period the seed clams were fed a 1% daily ration (% dry weight algae per wet weight clam per day) of the cultured diatom Chaetoceros muelleri . After 14 d of culture at the 1.0 g whole wet weight/cm² stocking density, seed clams (4.4 ± 0.6 mm initial shell length) under fluidized-flow condition exhibited better growth (0.54/d), and a greater final shell length (5.9 ± 1.0 mm). At the high density stocking conditions, after 28 d of culture, seed clams (4.2 ± 0.6 mm initial shell length) in the fluidized-flow culture conditions again exhibited better growth rate (0.031/d) and a greater final shell length (6.0 ± 1.0 mm). The preliminary evaluation of fluidized-flow for seed clam culture in land-based nurseries indicates its potential as a suitable alternative to raceway, downwelling, or traditional forced-flow culture methods.     

Growth of the hard clam Meretrix lusoria in Taiwan

The growth of hard clam Meretrix lusoria in Taiwan was observed as it was grown at six different stocking rates (55, 109, 172, 244, 344 and 455 clams/m²), from November 1979 to September 1980. It was found that the stocking rate had more effect on the increase of the total weight of the clam than on the shell length. Under the environmental condition of the study site, the optimum stocking rate was 244 clams/m². When the net production of the clam was lower than 1103 g/m², the growth of the individual clam was not affected by the stocking rate. But when the net production was higher than 1589 g/m², the growth of the individual clam seemed to be retarded. The average pH of the sea water in the clam culture area was between 7.9 and 8.4. The average dissolved oxygen content was between 4.2 and 11.2 mg/l. And the average water salinity was between 30‰ and 35‰. All these three factors did not seem to have direct relationship with the growth of the clams. Sea water temperature, however, showed great effects on the growth of the clams. It is shown that the growth of the hard clam was slow at a water temperature of 15–18°C, increased at 20–22°C, and accelerated at 25–32°C.     

文蛤浮游期发病幼虫细菌群落分析和致病菌的分离鉴定

为研究文蛤育苗过程中幼虫病害及其主要致病菌,实验通过构建细菌16S rDNA克隆文库、病原菌分离纯化、人工感染和药敏实验等方法对育苗场发病的浮游期文蛤壳顶幼虫样品进行了系统分析。结果显示,发病的文蛤壳顶幼虫细菌群落多样性低,地中海弧菌占比高达75%以上,推断其可能为引发此次幼虫发病的主要致病菌。从发病幼虫的匀浆组织中分离获得该优势菌株,测序及系统发育鉴定为地中海弧菌。人工感染实验确定了其致病性,菌株US2-01在1.0×10⁶ CFU/mL的菌液浓度下浸泡感染文蛤浮游幼虫,96 h累计死亡率为84%。药敏实验表明,地中海弧菌菌株US2-01在12种抗生素的测试中对常用的青霉素、氨苄西林、红霉素等抗生素具有一定的耐药性,对四环素和多西环素中度敏感,对头孢他啶、庆大霉素、卡那霉素等其余7种抗生素呈现高度敏感。本研究首次报道了地中海弧菌为文蛤浮游期幼虫致病的一种潜在病原,研究结果可为文蛤幼虫疾病研究及贝类苗种培育过程中的病害防控提供科学依据。     

Culture possibilities of the razor clam Ensis arcuatus (Pharidae: Bivalvia)

This study investigated razor clam Ensis arcuatus culture from larval rearing to commercial size to assess it's aquaculture potential. Broodstock was spawned several times in hatchery facilities to demonstrate that larval availability is not a constraint for hatchery production. Larval culture lasted 20 days, showing an average survival of 14.35%. The razor clam seed reached a size of 28.5 mm at 4 months. Seed culture is feasible; however, it is constrained by the fact that razor clams need to be buried. Higher survival was observed when culturing razor clam seed with a substrate (82–83%), irrespective of the substrate grain size, while containers held without a substrate showed a significantly lower survival (56.5%). We showed that it is possible to rear E. arcuatus juveniles in bottles, with survival as high as 94–95% being achieved. The length increase of the hatchery‐produced E. arcuatus over 600 days was described by the equation Ln L=4.5+(?141.17/t), where L is length in mm and t is time in days. On‐growing showed adequate survival rates and it took 2–3 years to reach commercial size.     

Culture of Juvenile Atlantic Surfclams, Spisula solidissima solidissima and Spisula solidissima similis, in Forced-Flow Upwellers in a Bivalve Hatchery in Coastal Georgia

Four experimental growth studies for juvenile Atlantic surfclams, Spisula solidissima solidissima and Spisula solidissima similis , under hatchery conditions were conducted in 10-cm diameter forced-flow upweller units. Experiments were designed to determine optimum food ration (2%, 5%, and 8% g dry weight of algae/g wet weight of clam), water culture temperature (20, 25, and 30°C), flow rate (2, 4, and 6 Lpm), and stocking density (7, 14, and 21 g wet weight of clams) for rearing juvenile clams in upweller units. Each experimental trial was performed for a 14-d period. Nested Analysis of Variance showed that juvenile surfclams Spisula solidissima similis grew significantly faster at a temperature of 20°C and food rations of 5 % and 8%. In all four experiments, clam mortalities were not observed except in the temperature experiment, where total mortality occurred for clams cultured at 30°C. Clam growth in biomass and size decreased significantly with increases in culture temperature. For Spisula solidissima solidissima , clam growth was significantly reduced in terms of size and biomass at a flow rate of 6 Lpm. No difference in size or biomass was determined between clams grown at a flow rate of 2 or 4 Lpm. Surfclams at the lowest stocking density of 7 g wet weight significantly increased more in net biomass compared to those at higher stocking densities. Clams were significantly larger in shell length when grown at the two lower stocking densities compared to those at the highest stocking density. Hatchery-rearing protocol for juvenile surfclams is discussed.     

Abundance and culture trials of Ruditapes philippinarum (Adam and Reeve, 1850), and abundance of Tellina (Quidnipagus) palatum (Iredale, 1929) at two sites in Kāne'ohe Bay,O'ahu,Hawai'i

Abundance, length‐frequencies and distribution of Ruditapes philippinarum (Manila Clams) and Tellina (Quidnipagus) palatum were measured at two beaches in Kāne'ohe Bay, O'ahu, Hawai'i in June, 2010. Abundances had decreased from 866.2 m^?2 to 3.4 m^?2 for Ruditapes and from 75.5 m^?2 to 1.5 m^?2 for T. palatum since 1977. Distribution of both species was patchy, but both were most commonly found >40 m from shore. Size frequencies of live clams compared with empty shells suggest that few Ruditapes survive to sexual maturity. A similar trend was not detected for T. palatum. Aquaculture trials of R. philippinarum were conducted at the He'eia and Moli'i traditional Hawaiian fishponds in the same bay. The clams failed to thrive, although triploid and diploid Crassostrea gigas performed well in concurrent trials in the same fishponds. Current lower abundances for wild R. philippinarum could be due to factors related to predation or nutrient limitations. Previously, two large sewage outfalls existed at the surveyed clam bed areas which may have temporarily increased nutrient availability for both wild and cultured clams. Current nutrient levels may inhibit Manila clam growth and recruitment in Kāne'ohe Bay.     

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.     

胶州湾移植底播菲律宾蛤仔的生长和死亡特性

2004年5月至2005年4月对胶州湾菲律宾蛤仔（Rudimpes philippinarum）底播增殖区进行了逐月定点采样，将样品带回放于实验室内水族箱暂养，每站随机取样，共对3269个个体进行了基本生物学特性测定，研究了移植底播菲律宾蛤仔的生长、死亡等渔业生物学特性。结果表明，底播增殖菲律宾蛤仔苗种的平均个体质量0．26g、平均壳长11．1mm；底播蛤仔与野生蛤仔在生长规律上基本一致，春末至秋初（4～9月）是其主要生长期；1～3龄期间个体生长速度较快，1～2龄、2～3龄，个体质量分别增长3．88g和4．02g；1～2龄生物量增长最快，2～3龄由于死亡率增大，其生物量增长缓慢；1～3龄蛤仔软体部的生长速度快于贝壳，5～6月是菲律宾蛤仔的繁殖肥育期。根据个体生长特性，3龄为最佳采捕年龄；根据目前的养殖状况，2龄蛤仔已达到商品规格，从生物量上分析，采捕2龄蛤仔收益最高；6月是最佳的捕获时期。蛤仔生长具有明显的季节变化，水温是影响菲律宾蛤仔生长的主要环境因子。[中国水产科学，2006，13（4）：642—649]     

Waste excretion characteristics of Manila clams (Tapes philippinarum) under different temperature conditions

Water recirculating systems have been used in the shellfish industry for depuration and wet-storage. Knowledge of shellfish excretion characteristics is critical to recirculating system design. In this study, the excretion rate of total ammonia nitrogen (TAN), total Kjeldahl nitrogen (TKN), and 5-day biochemical oxygen demand (BOD₅) from Manila clams (Tapes philippinarum) were investigated under both laboratory and commercial conditions. The laboratory tests were conducted under temperatures ranging from 3 to 30°C. The experimental results showed that temperature was a key factor in determining the excretion rate of all the above parameters. The relationship between TAN excretion rate (R_TAN) and temperature (T) can be represented by an exponential function (R_TAN=0.57×1.25^T). For the temperature range between 3 and 20°C, the daily mean excretion rates of TAN, TKN and BOD₅ ranged between 1.5–46.1, 4.8–131.0 and 57.4–219.4 mg per kilogram of the clams (wet weight with shell on), respectively. There were linear correlations between TAN, TKN and BOD₅ production rates. The data presented in this paper can be used to estimate waste generation from a given shellfish processing operation and to size the waste treatment components for a recirculating depuration (or wet-storage) system.     

Studies on aneuploid pearl oyster (Pinctada martensii Dunker) produced by crossing triploid females and a diploid male following the inhibition of PB1

Viable aneuploid embryos of pearl oyster, Pinctada martensii Dunker, were produced by inhibiting the first polar body (PB1) with cytochalasin B treatment in eggs from triploids fertilized with haploid sperm. During the period of growth measurement, aneuploid showed the slowest growth compared with diploid and triploid groups. The body size and weight measurement data showed that there were no differences between aneuploids (as a group) and diploids in body size and weight (P>0.10), but that they were significantly different from triploids (P<0.01). There were no differences between aneuploids within diploid condition (2n±n) and diploids in SL (P>0.1), but significant differences in BW were found (P<0.05). Aneuploids within triploid condition (3n±n) were significantly smaller than triploids in BW (P<0.05), but not different from triploids in SL (P>0.05), and almost identical to diploids in both (P>0.1). These dada indicated that some aneuploids might be associated with growth retardation. Karyotype analysis revealed that there were metacentric, submetacentric or subtelocentric chromosomes losses or gains; aneuploid pearl oysters with the same chromosome numbers had different chromosome composition. Aneuploids are valuable research materials for genetic analysis.     

Studies on triploid oysters in Australia: effect of initial size on growth of diploid and triploid Sydney rock oysters, Saccostrea commercialis (Iredale & Roughley)

In a 2-year grow-out trial, triploid Sydney rock oysters, Saccostrea commercialis (Iredale & Roughley), from two initial size grades grew faster (in terms of both mean whole weight and shell height) than the equivalent initial size grades of sibling diploids (P < 0.05). Small size grade triploids caught up with and had significantly heavier (P < 0.05) final whole weights than large size grade diploids after a 2-years grow-out period. The initial size grade had a significant effect on final mean whole weight and shell height for both ploidy types. After the 2-years grow-out trial, the final mean whole weights (but not shell heights) of small and large diploids (35.8 ± 0.6 g and 39.4 ± 0.5 g, respectively) were significantly different (P < 0.05). Small and large triploids grew at a similar rate for the first 18 months despite the significantly (P < 0.05) heavier final mean weight of large grade triploids (48.4 ± 0.8 g and 61.2 ± 0.7 g, respectively). The effect of the initial size grade on subsequent growth of both diploid and triploid oysters which was demonstrated in the present study is of significant commercial value to hatchery and nursery operators as well as growers of single seed oysters. In addition, small-grade triploids appeared to be more valuable in terms of potential growth rate than all diploid grades. There was no significant difference in the final percentage triploidy between small and large grade triploids. A large proportion of diploid/triploid mosaicism was detected in adult oysters.     

Prey preference of Carcinus aestuarii: possible implications with the control of an invasive mytilid and Manila clam culture in a northern Adriatic lagoon

The cultivated Manila clam, Ruditapes philippinarum, and the accidentally introduced Asian date mussel, Musculista senhousia, are nowadays the most abundant bivalve species in the Sacca di Goro (northeastern Italy). M. senhousia, with its sub-surficial extended mats, creates quite a heavy economical impact to clam shellfish culture. Individual Mediterranean shore crabs Carcinus aestuarii were allowed to forage on the two bivalve species to examine the crab's preference in light of the optimal foraging theory. Crabs preferred M. senhousia over R. philippinarum: mortality was higher for the former (34.6%) than for the latter bivalve species (9.5%). It is suggested that the marked preference of C. aestuarii for Asian date mussels over Manila clams could be advantageously exploited to control or to reduce the extension of mats, especially where these create management problems to infaunal, burrowing bivalve cultures.