ALBERT

Notes: Practical diets designed for penaeid shrimp are commonly supplemented with phosphorus, which may lead to unnecessary nutrient loading of the culture system and effluent waters as well as unnecessary investments in a nutrient that is not utilized by the culture species. To facilitate the optimization of phosphorus levels in practical shrimp feeds, research was conducted with Penaeus vannamei juveniles to determine the biological availability of two feed-grade calcium phosphate sources. A practical basal diet containing 350 g protein kg−1 diet and 9.8 g P kg−1 diet was formulated using anchovy and soybean meal as the primary protein and phosphorus sources. The basal diet was supplemented with graded levels of phosphorus and offered to juvenile shrimp (0.57 ± 0.017 g) over a 10-week period. Weight gain and estimated feed efficiency values increased with phosphorus supplements, indicating a dietary deficiency of the basal diet. Under the reported conditions, a dietary supplement of 1.4 or 2.3 g P kg−1 diet was required for maximum growth and estimated feed efficiency values if Cefkaphos (primarily monobasic calcium phosphate) or Dynafos (primarily dibasic calcium phosphate) was utilized. Dynafos was determined to have a relative biological value (RBV) of 63.8% of Cefkaphos based on final weights of the shrimp offered diets containing 1.25 g supplemental P kg−1 diet. A similar RBV of 60.9% was estimated based on broken-line analyses of growth data. There were no significant differences in apparent net phosphorus retention (ANPR) for the basal diet (23.1%) or diets supplemented with 1.25 g P kg−1 diet originating from Cefkaphos (25.7%) or Dynafos (17.9%). However, shifts in ANPR values of the diets corresponded to biological availability of the two phosphorus sources.

Notes: A series of growth trials was conducted to evaluate the use of soy protein as a replacement for fish protein in isonitrogenous practical diets for juvenile red drum Sciacnops ocellatus. Feeds were offered at or in excess of satiation to juvenile red drum maintained at 26–28 C and a salinity of 25–35 ppt. In the first growth trial, red drum were offered one of four diets containing graded levels of menhaden fish meal, replacing solvent-extracted soybean meal and soy-protein isolates. Differences in weight gain, survival and feed efficiency ratios of the fish corresponded to increases in fish meal content of the diets. Due to poor performance of the fish maintained on the low (15%) fish meal diet, a methionine supplement was introduced into this diet at the midpoint of the growth trial. A positive increase in growth indicated a dietary deficiency of methionine and/or total sulfur amino acids in the unsupplemented diet. A positive response to dietary fish meal also occurred in the second growth trial despite the supplementation of L-methionine in the test diets. In low fish meal diets the utilization of solvent extracted soybean meal or a soy-protein isolate resulted in similar growth responses. Hence, the presence of an antinutrient did not likely cause reduced growth rates. In the third feeding trial, weight gain also increased with increasing fish meal content of the diet despite the equalization of digestible protein and selected amino acids. There were no significant differences in whole-body compositions which indicated similar biological value of the diets (protein digestibility, amino acid balance and energy availability). The singular deletion of fish-solubles, glycine, lysine and methionine from the diet containing the lowest level of fish meal (10 g/100 g diet) did not result in significant changes in weight gain. This indicated that these components did not add to the nutritive value and/or palatability of this formulation. The final experiment was designed to evaluate the response of red drum to a control diet (high fish meal) as compared to a low fish meal diet with and without potential attractants/palatability enhancers. Weight gain and feed efficiency ratios of fish offered the low fish meal diet supplemented with seafood flavor or fish flavor #2 were not significantly different from the control (high fish meal diet). Based on the results of this study, with suitable formulation restrictions, soy protein is acceptable for inclusion in practical diet formulations for red drum. However, soy protein itself does not appear replete in sulfur-containing amino acids and does not have acceptable palatability properties. Consequently, feeds containing reduced levels of marine proteins could require suitable attractants and/or amino acid supplements.

Notes: Experiments were conducted to determine the dietary zinc requirement of Penaeus vannomri and evaluate the effects of phytate on zinc bioavailability. Prior to initiation of the growth trial, 20-day-old P. vonnamei postlarvae (mean weight 0.0032 g) were fed a casein-gelatin based semi-purified diet lacking zinc supplementation but containing 18 mg Zn/kg diet for one week. Subsequently, juveniles (mean weight 0.058 g) were fed one of seven diets containing either supplemental zinc (0, 15, 30, 60 mg/kg diet) without phytate or supplemental zinc (0, 60, 200 mg/kg diet) with 1.5% phytate for 33 days. Weight gain was greatest in shrimp fed 15 mg supplemental Zn/kg diet. In the absence of dietary phytate, zinc concentrations in the hepatopancreas of shrimp were maximized when zinc was supplemented at levels greater than or equal to 15 mg Zn/kg diet (33 mg total Zn/ kg). Supplementation of 1.5% phytate to the diet did not have a significant effect on growth or zinc concentrations in the carapace; however, it did depress zinc levels in the hepatopancreas. Supplementation of 200 mg Zn/kg diet was required to overcome the depressed bioavailability of zinc caused by the presence of dietary phytate and return zinc levels of the hepatopancreas to that observed when phytate was not present. Based on apparent digestibility values phytate phosphorus was unavailable to the shrimp and the presence of phytate depressed the bioavailability of phosphorus and zinc.

Notes: Techniques for head starting or nursing postlarvae (PL) has received considerable attention with regards to nursery protocols, yet there is little data pertaining to the effects of nursery period on the final growout of shrimp to marketable size. This study was performed to investigate the influence of nursery duration on survival and growth of Litopenaeus vannamei during subsequent pond culture. For this research, a single population of high health PL were received from a commercial hatchery and held in a tank for acclimation, quantification, and distribution to nursery tanks or ponds. Treatments included direct stocking of 10-d-old postlarvae (PL10) into production ponds as well as the nursing of PL in a covered greenhouse nursery system for an additional 10 or 20 d. After nursing, the PL were harvested, quantified, and transferred to growout ponds. All ponds were stocked at a density of 35 PL/m2 and maintained under standardized conditions. Shrimp were fed with a 35% protein shrimp feed, twice daily during the 112-d growth trial. Ponds were aerated as needed using a maximum of 19 hp/ha to maintain adequate dissolved oxygen (DO 〉 3.0). No statistical differences (P 〉0.05) were found in survival, yield, or growth between treatments. At harvest, survivals during growout were generally higher in ponds with nursed shrimp (77% for PL20 and 79% for PL30) than in ponds receiving PL10 shrimp (67%). Yields were similar between treatments, ranging from 3,525 for direct stocked shrimp to 3,747 kg/ha for those that were nursed for 10 d. Although growth rates of PL under pond conditions will be faster than that of a nursery system, results suggest that a nursery period of at least 10 d helps improve survival during pond production and promotes better size uniformity. Shrimp nursed for 20 d showed little improvement in survival over shrimp nursed for 10 d but did result in a more uniform size of shrimp at harvest.

Notes: This research evaluated ozone treatment of three unicellular algal species commonly used in the culture of marine larvae. Isochrvsis galbana and Nannochloropsis oculata were found to be resistant to total residual oxidants (TRO); whereas, Chaetoceros gracilis was relatively sensitive to TRO. Isochrvsis galbana remained in log-phase growth after treatment with 0.05 mg/L to 0.50 mg/L TRO, and N. oculata exhibited strong growth after being exposed to TRO levels up to 0.67 mg/L. Only TRO levels of 0.92 mg/L and 0.90 tng/L reduced cell counts of N. oculata and I. galbana, respectively. Furthermore, algal cultures having higher concentrations at the time of ozone treatment may respond more favorably to the treatment. Initially, C. gracilis was reduced in cell count at TRO levels above 0.06 mg/L, but log-phase growth was resumed 2 d after exposure to TRO levels as high as 0.31 mg/L. It is concluded that I. galbana and N. oculata can be successfully treated with ozone in the mass production stages without hampering the timely production of concentrated cultures. Although C. gracilis was found to be relatively sensitive, ozone treatment of starter cultures can be performed routinely with this species. We have demonstrated that ozone treatment of algal cultures is a feasible technique, but studies need to be conducted on ozone treatment of other species of unicellular algae and on ozone treatment of varying concentrations of algae in order to enhance the applications of this technique. Also, in order to determine the extent of disinfection of algal cultures, bacterial and viral composition of the cultures should be evaluated in future studies.

Notes: Abstract— The purpose of this study was to examine the effect of varying dietary levels of highly unsaturated fatty acids (HUFA) in Live prey on the standard length, specific growth rate, survival, and fatty acid composition of yellowtail snapper Ocyurus chrysurus larvae. Two experiments were conducted utilizing rotifers and Artemiu enriched with live algae (Isochrysis galbana or Nannochloris oculata) or commercial preparations (Aquagrow Advantage, Aquagrow Advantage plus Aquagrow arachidonic acid, and Algarnac 2000). Larval growth and fatty acid composition were evaluated during the rotifer, Brachionus plicatilis, and Artemia feeding periods and survival rates were calculated at the termination of each trial (18 or 20 d after hatching). In general, prey enriched with the commercial products contained higher levels of docosahexaenoic acid, eicosapentaenoic acid, n-3 HUFA, and × HUFA than those enriched with live algae. The addition of arachidonic acid to the Aquagrow Advantage enrichment medium significantly increased the amount of this fatty acid in rotifers but not in Artemia. At the end of the growth trials, larval standard length was highest when larvae were fed prey enriched with I. galbanu (6.4 mm) or commercial preparations (6.7–7.1 mm) versus N. oculatu (5.2 mm). Furthermore, larvae fed prey enriched with commercial preparations had significantly (P 〈 0.05) higher survival rates (2.2-5.9%) than those fed prey enriched with live algae (1.1-1.4%). These results suggest that yellowtail snapper larvae require dietary levels of HUFA beyond those achieved by enriching prey with live N. oculata or I. galbana

Notes: Shrimp farmers have access to and have evaluated a diverse number of shrimp species; however, due to culture and market considerations three penaeid species (Penaeus monodon, P. orientalis and P. vunnamei) account for 80% of the world production (Weidner and Rosenbeny 1992). Although culture techniques for these species have been extensively studied and are relatively well established, they are not native to U.S. coastal waters and hence possess problems associated with the use of exotic species. Three native species P. aztecus. brown shrimp; P. duorarum, pink shrimp; and P. setiferus, white shrimp, support commercial fisheries along the Gulf states (Gulf of Mexico Fishery Management Council 1981). The commercial culture of these species would avoid the inherent problems associated with the culture of exotic species and allow shrimp farmers in the Caribbean basin to more effectively expand operations.

Notes: Diets containing a complete mineral premix or mineral premixes from which Ca, P, Na, CI, K, Mg, Mn, Fe, Zn, Cu, I, Se, or Cr were individually deleted were fed to juvenile Penaeus vunnamei (mean initial weight 79.5 mg) over a 4-week experimental period. Final mean percent weight gain ranged from 1,472 (Cu-free mineral premix) to 1,991% (Na-free mineral premix) with an average of 1,812% for all treatments. Survival during the first two week period and the second two week period was greater than 92% and 88%, respectively. There were no significant differences observed among treatments for growth and survival data.Upon termination of the growth trial, the hepatopancreas and carapace were dissected from the shrimp and evaluated for ash, Ca, P, Na, K, Mg, Mn, Fe, Zn and Cu content. Of the minerals analyzed, the individual deletion of Mg, Mn, Fe, Zn and Cu from the mineral supplement resulted in reduced tissue mineralization in P. vannamei whereas, the deletion of Ca and P from the mineral mix did not produce significant responses. Deletion of Se from the mineral premix resulted in a significant increase in the ash content of the carapace. Based on the information provided by this and other studies, further investigation of the dietary requirements of P. vannamei for Ca, P, Fe, Mg, Mn, Zn, Cu and Se is recommended.

Notes: Quadruplicate groups of juvenile red drum (initial mean weight 2.7 g; 20 fish per replicate) were fed experimental diets containing 35% crude protein and graded levels of lysine for eight weeks. Lysine concentration in the basal diet was 1.2% and was supplied by a combination of peanut meal and shrimp-head meal. The basal diet was supplemented with lysine-HCI to provide 1.6, 2.0, and 2.4% lysine. Each of these diets contained an essential amino acid (EAA) premix. Two additional diets were formulated to contain 1.2 and 2.4% lysine without the EAA premix. Weight gain and feed efficiency (FE) data indicated between 1.2 and 1.6% dietary lysine was adequate. However, serum lysine concentrations indicated 1.6–2.0% lysine was required. Fish fed 1.2 or 2.4% lysine, without the EAA premix, exhibited reduced weight gain and feed efficiency. Results indicated that red drum were able to utilize crystalline amino acids when incorporated into diets containing intact protein and, when lysine was adequate, the proteins were deficient in at least one other essential amino acid. It is recommended that a dietary lysine level of 5.7% of the dietary protein be used in formulating red drum diets.

Notes: Quadruplicate groups of juvenile red drum (initial mean weight 2.7 g; 20 fish per replicate) were fed experimental diets containing 35% crude protein and graded levels of lysine for eight weeks. Lysine concentration in the basal diet was 1.2% and was supplied by a combination of peanut meal and shrimp-head meal. The basal diet was supplemented with lysine-HCl to provide 1.6, 2.0, and 2.4% lysine. Each of these diets contained an essential amino acid (EAA) premix. Two additional diets were formulated to contain 1.2 and 2.4% lysine without the EAA premix. Weight gain and feed efficiency (FE) data indicated between 1.2 and 1.6% dietary lysine was adequate. However, serum lysine concentrations indicated 1.6-2.0% lysine was required. Fish fed 1.2 or 2.4% lysine, without the EAA premix, exhibited reduced weight gain and feed efficiency. Results indicated that red drum were able to utilize crystalline amino acids when incorporated into diets containing intact protein and, when lysine was adequate, the proteins were deficient in at least one other essential amino acid. It is recommended that a dietary lysine level of 5.7% of the dietary protein be used in formulating red drum diets.