319 research outputs found

    Closed System Culture of Penaeus vannamei

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    Penaeus vannamei were cultured utilizing three different closed recirculating seawater systems. The first system used biological filtration for water treatment. The second system utilized both physical and chemical filtration, but no biological filtration. The third system used a combination of biological, physical, and chemical filtration. Shrimp growth was monitored for a 12-week period for each system. Shrimp from the biological filtration system had a growth rate of 0.82 g/wk and an overall survival rate of 45.6%. Shrimp from the closed system which used physical and chemical filtration had a growth rate of 0.99 g/wk and a survival rate of 29.2%. In the third system which combined both types of filtration, the shrimp growth rate averaged 0.65 g/wk and the survival rate was 56.9%

    Comparing Salinities of 10, 20, and 30% in Intensive, Commercial-Scale Biofloc Shrimp (\u3ci\u3eLitopenaeus vannamei\u3c/i\u3e) Production Systems

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    Minimal-exchange, intensive biofloc aquaculture systems offer a viable means of culturing marine animals at inland locations due to very low rates of water use. Fresh, never-frozen shrimp can be provided to metropolitan markets; however, the cost of artificial salt can be substantial. The purpose of this project was to examine commercial-scale biofloc shrimp production at three different salinities. Nine raceways were randomly assigned to three salinity treatments: 10, 20, and 30‰ (LS, MS, and HS), each treatment contained three raceways operated at 50 m3. The raceways were operated as heterotrophic biofloc systems, with daily additions of sucrose to raise the C:N ratio. Temperature, dissolved oxygen, pH, and salinity were all maintained at consistent levels. Spikes of ammonia and nitrite occurred in all tanks but nitrate remained low, with a peak value of 8.7 mg NO3-N L− 1. There were no significant differences in any shrimp production metric. Mean shrimp growth rate was 1.8, 2.0, and 2.0 g week− 1 in the LS, MS, and HS treatments respectively. Mean feed conversion rate was 1.6, 1.2, and 1.2 in the LS, MS, and HS treatments respectively, and mean final weight ranged from 17.8 to 19.3 g. The only time water was removed from the systems was when settling chambers were emptied, resulting in a total mean water replacement of 5.2% or less per raceway. The mean volume of full strength seawater used to produce shrimp was 104, 159, and 235 L kg− 1 of shrimp in the LS, MS, and HS treatments respectively. Although there were no significant differences in shrimp production metrics between treatments, these values were noticeably lower in the LS treatment due to human error. Operating at the low salinity of 10‰ reduces salt use by about 50% over the MS treatment which implies substantial cost savings for production facilities. This study helps to illustrate the range of salinity options for shrimp production in commercial-scale biofloc systems

    Closed System Culture of Penaeus vannamei

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    Penaeus vannamei were cultured utilizing three different closed recirculating seawater systems. The first system used biological filtration for water treatment. The second system utilized both physical and chemical filtration, but no biological filtration. The third system used a combination of biological, physical, and chemical filtration. Shrimp growth was monitored for a 12-week period for each system. Shrimp from the biological filtration system had a growth rate of 0.82 g/wk and an overall survival rate of 45.6%. Shrimp from the closed system which used physical and chemical filtration had a growth rate of 0.99 g/wk and a survival rate of 29.2%. In the third system which combined both types of filtration, the shrimp growth rate averaged 0.65 g/wk and the survival rate was 56.9%

    Effects of Salinity on Survival and Growth of Postlarval Penaeus vannamei

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    Eight and 22-day-old Penaeus vannamei postlarvae were exposed to several salinities for 24 hours and 120 hours by direct transfer from 32 ppt salinity to lower salinity waters. The challenge study included six experiments conducted on 8-day-old postlarvae (PL-8) and five experiments conducted on 22-day-old postlarvae (PL-22). Each experiment consisted of ten replicates of ten animals each. Shrimp were held in 1 L plastic containers with 500-ml of seawater. Lowered salinity resulted in lower survival for shrimp of both ages. Longer exposure time resulted in lower survival for shrimp of both ages. Younger shrimp exhibited lower survival than older shrimp. Survival of 8-day-old postlarvae after 24-hour exposure to salinities of 32, 16, 8, 4, and 2 ppt was 97.3%, 92.8%, 19.8%, 8.2% and 1.7%, respectlvely. Survival of 22-day-old postlarvae after 24-hour exposure was 99.2%, 97.8%, 83.8%, 63.4% and 40.2%, respectively. A second series of experiments investigated the effect of salinity upon growth of 22-day-old postlarvae which had been acclimated to four different salinities (16, 8, 4, and 2 ppt). Thirty shrimp were stocked in triplicate into 113 L (30 gal) aquaria and fed a prepared commercial feed. Growth was determined after 30 days at 16oC and 28-30oC. Growth was greatest at higher temperatures, but statistically significant differences due to salinity were not detectable. Nonetheless, best observed growth occurred at the intermediate salinities of 8 and 4 ppt

    Gonadal Maturation in the Cobia, Rachycentron canadum, from the Northcentral Gulf of Mexico

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    Gonadal maturation of cobia, Rachycentron canadum, was evaluated by examining 508 specimens from its recreational fishery. Specimens were collected off southeast Louisiana to northwest Florida by hook-and-line during February through October 1987-1991. Fork lengths (FL) of these fish ranged from 580-1,530 mm, with corresponding weights of 2.0-43.5 kg. The female:male ratio was 1:0.37. Using a combination of oocyte size frequency and histological assessment of many of the fish, we determined that females were ripe from May through September, with atretic oocytes occurring in some fish from July through October. Degenerating hydrated oocytes in July and October and the presence of resting ovaries in July suggest two major spawning periods; however, monthly gonosomatic indices peaking in May, followed by a steady decline, do not support that finding. Ovaries were placed into undeveloped, early developing, mid-developing , or late developing categories based upon oocyte size-frequency distributions. Developing ovaries had two or three modes of oocytes larger than 30 pm. Batch fecundity was estimated to be 2.6x106 to 1.91x108 oocytes, depending on the size of fish/ovaries. The smallest female with oocytes exhibiting vitellogenesis was 834 mm FL. This fish was 2 years old based its otolith evaluation. The smallest male with an abundance of spermatozoa in its testes was 640 mm FL and 1 year old based on otolith evaluation; smaller males were not examined. Females larger than 840 mm FL had vitellogenic oocytes in March and April. A few fish still had vitellogenic oocytes in early October, but none did by late October. When Gilson’s fluid was used to assess ovarian tissue, the fresh weight of the tissue was reduced by 20% after being stored for 3 months. The diameter of oocytes shrunk about 25% in Gilson’s fluid which was 11% less than those fixed in formalin, embedded in paraffin, and sectioned. Tissue sections from specific individuals, each demonstrating a variety of different developmental stages, were similar regardless of whether they were obtained from the anterior, middle, or posterior portion of either ovary

    Gonadal Maturation in the Cobia, Rachycentron canadum, from the Northcentral Gulf of Mexico

    Get PDF
    Gonadal maturation of cobia, Rachycentron canadum, was evaluated by examining 508 specimens from its recreational fishery. Specimens were collected off southeast Louisiana to northwest Florida by hook-and-line during February through October 1987-1991. Fork lengths (FL) of these fish ranged from 580-1,530 mm, with corresponding weights of 2.0-43.5 kg. The female:male ratio was 1:0.37. Using a combination of oocyte size frequency and histological assessment of many of the fish, we determined that females were ripe from May through September, with atretic oocytes occurring in some fish from July through October. Degenerating hydrated oocytes in July and October and the presence of resting ovaries in July suggest two major spawning periods; however, monthly gonosomatic indices peaking in May, followed by a steady decline, do not support that finding. Ovaries were placed into undeveloped, early developing, mid-developing , or late developing categories based upon oocyte size-frequency distributions. Developing ovaries had two or three modes of oocytes larger than 30 pm. Batch fecundity was estimated to be 2.6x106 to 1.91x108 oocytes, depending on the size of fish/ovaries. The smallest female with oocytes exhibiting vitellogenesis was 834 mm FL. This fish was 2 years old based its otolith evaluation. The smallest male with an abundance of spermatozoa in its testes was 640 mm FL and 1 year old based on otolith evaluation; smaller males were not examined. Females larger than 840 mm FL had vitellogenic oocytes in March and April. A few fish still had vitellogenic oocytes in early October, but none did by late October. When Gilson’s fluid was used to assess ovarian tissue, the fresh weight of the tissue was reduced by 20% after being stored for 3 months. The diameter of oocytes shrunk about 25% in Gilson’s fluid which was 11% less than those fixed in formalin, embedded in paraffin, and sectioned. Tissue sections from specific individuals, each demonstrating a variety of different developmental stages, were similar regardless of whether they were obtained from the anterior, middle, or posterior portion of either ovary
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