A Preliminary Study on the Effects of Salinity on Growth and Survival of Mulloway Argyrosomus japonicus Larvae and Juveniles

Abstract.— Tko experiments were conducted to determine the effects of salinity on growth and survival of mulloway Argyrosomus japonicus larvae and juveniles. First, 6-d-old larvae were stocked into different salinities (5, 12.5, 20, 27.5 and 35 ppt) for 14 d. Larvae grew at all salinities, but based on results for growth and survival, the optimum range of salinity for 6-d-old to 20-d-old larvae is 5–12.5 ppt. During this experiment larvae held in all experimental salinities were infested by a dinoflagellate ectoparasite, Amyloodinium sp. Degree of infestation was affected by salinity. There were very low infestation rates at 5 ppt (0.2 parasites/larva). Infestation increased with salinity to 20 ppt (33.1 parasites/larva), then declined with salinity to 35 ppt (1.5 parasites/larva). For the second experiment, juveniles (6.1 ± 0.1 g/fish) were stocked into different salinities (0.6, 5, 10, 20 and 35 ppt) for 28 d. Juveniles were removed from freshwater 3 d after transfer as they did not feed, several fish died and many fish had lost equilibrium. However, when transferred directly to 5 ppt. these stressed fish recovered and behaved normally. Trends in final mean weight and food conversion ratio of juvenile mulloway suggest that fish performed best at 5 ppt. Although salinity (5 to 35 ppt) had no significant ( P > 0.05) effect on growth, survival, or food conversion ratio of juveniles, statistical power of the experiment was low (0.22). Based on these results we recommend that mulloway larvae older than 6 d be cultured at 5 to 12.5 ppt. Optimum growth of juveniles may also be achieved at low salinities.     

Survival and Growth of White Bass Morone chrysops Reared at Different Salinities

Abstract.— Juvenile white bass Morone chrysops (age 158 d, 110.4 mm total length) were reared at salinity levels of 0, 4, 8, 12, 16, and 20 parts per thousand (ppt). Fish (10/tank) were stocked in 64-L tanks with four replicates/treatment ( N = 40heatment) and fed a pelleted feed daily. Fish were sampled semimonthly for 70 d. Fish reared at salinities of 12 ppt and below were significantly ( P ≤ 0.05) larger (mean = 151.5 mm total length; range 146.8–155.7 mm) than fish reared at salinities of 16 and 20 ppt (mean 133.7 mm total length; range 131.5–135.8 mm) after 70 d. Survival was also higher ( P ≤ 0.05) among fish reared at salinities of 12 ppt or lower (mean 85.6%; range 77.5%–92.5%) compared to those reared at the two highest salinities (42.5% survival at 16 ppt; 5.0% survival at 20 ppt). Thus, although typically found in freshwater habitats, white bass can survive and grow in brackish water.     

The effect of salinity on growth and survival of juvenile black bream (Acanthopagrus butcheri)

Growth and survival of juvenile black bream (Acanthopagrus butcheri) were determined at salinities from 0 to 60 ppt (in 12-ppt increments) and from 0 to 12 ppt (in 4-ppt increments) in two separate trials of 6 and 4 months duration, respectively. Juvenile black bream were able to survive and grow at salinities ranging from freshwater (0 ppt) to 48 ppt. Osmotic stress was evident at 60 ppt, however, survival was not significantly affected. Fish reared at 24 ppt in trial 1 had a specific growth rate of 2.34±0.03%/day, a rate significantly higher only to those fish reared at 60 ppt (2.16±0.04%/day). Growth was greater at 24 ppt in association with the highest food intake and most efficient FCR. Although both food intake and FCR were not significantly higher than those obtained with fish reared at 12, 36 and 48 ppt, the combination of the two factors being optimised at 24 ppt lead to the greatest growth. Analysis of data from the second trial found no significant difference in the growth rate of black bream reared at salinities ranging from freshwater to 12 ppt, with SGR ranging from 1.92±0.05%/day to 2.05±0.02%/day. Variable results in freshwater between the two trials suggested that total hardness of freshwater may influence survival and/or an ontogenetic change in salinity tolerance may occur.     

Growth of Tiger Puffer, Takifugu rubripes, at Different Salinities

Two 12‐wk rearing experiments were conducted to examine the effect of rearing salinities of 10–35 ppt on the growth of 3‐ and 170‐g‐size tiger puffer, Takifugu rubripes. Fish were reared in a closed recirculation system without introducing fresh culture water at 23 C and were fed commercial pellet diet for tiger puffer twice or three times daily to apparent satiation each, almost everyday. Growth of 3‐g‐size fish seemed to increase with decreasing salinity; however, there were no significant differences in the specific growth rate and weight gain among treatments because of differences in initial body weight. Final body weight and length of fish reared at 10 ppt were significantly higher than those for fish reared at 30 ppt although initial sizes were similar. Differences were not found for the feed efficiency (FE) and daily feed consumption. Apparent relationships were not observed between salinity and blood characteristics or proximate compositions of muscle of the cultured fish. Differing from smaller fish, growth of 170‐g‐size fish tended to decrease with decreasing salinity from 30 to 10 ppt and with increasing salinity from 30 to 35 ppt. Similar trends for FE were observed.     

Salinity Effects on Early Life Stages of Southern Flounder Paralichthys lethostigma

Abstract.— In South Carolina, studies have been conducted to develop rearing techniques for southern flounder Paralichthys lethostigma a candidate for aquaculture development and stock enhancement programs. To help define environmental tolerances, a variety of salinity studies were conducted with the early life stages of this species. Eggs were buoyant at 32 ppt and sank at 29 ppt with salinities of 30–31 ppt providing varying levels of suspension in the water column. Eggs incubated at 0 and 5 ppt all died, whereas 82.5% hatched at 10 ppt but larvae died shortly thereafter. At 63 h post-fertilization, there were no differences in hatch level for eggs incubated at salinities of 15 to 35 ppt (mean hatch level 98.5%). In a 72-h study, fish 3 wk post-metamorphosis (13.7 mm TL, 50-d-old) were acclimated to seven salinities ranging from 0–30 ppt. Fish held at 0 ppt salinity exhibited a statistically (P < 0.05) lower survival (20.0%) than those exposed to 5–30 ppt salinity concentrations. No differences were detected in survival (mean 99.1%) among fish held in the higher salinities. A second study examined the tolerance of older juveniles to lower salinities. Juvenile flounder (95.2 mm TL, 220-d-old) were acclimated to 0, 1,5 and 10 ppt salinities and reared for 2 wk. Results showed that fish could tolerate salinities of 0–10 ppt (100% survival). These data indicate that salinity tolerance of southern flounder increases with age. In addition to the short duration studies, a replicated 11-mo duration tank grow-out study was conducted at mean salinity 5.4 ppt and mean temperahue 22.6 C with an all male population. Flounder grew from a mean length of 100 mm to 213 mm TL and weight from 8.9 to 104.3 g. Growth of the cultured fish approximated that observed among male flounders in the wild.     

Effects of Nitrite Exposure on Growth and Survival of Sea Bass,Lates calcarifer,Fingerlings in Various Salinities

Sea bass, Lates calcarifer, fingerlings were acclimated to 0. 15, and 32 ppt, and the toxic effects of nitrite exposure were assessed. The 96-hour median lethal concentrations (96-hour LC₅₀ for nitrite were estimated to be 14.5 mg/L at 0 ppt, 105 mg/L at 15 ppt and 93 mg/L at 32 ppt salinity. Chronic exposure to a nitrite concentration equivalent to 10% of the respective 96 hour LC₅₀ resulted in marked growth reduction: growth being reduced in the order of 0 ppt > 32 ppt > 15 ppt. In nitrite-free water, growth rate for fish raised at a salinity of 15 ppt was higher compared to fish raised at salinities of 0 ppt and 32 ppt, a phenomenon which probably reflected the advantage of a reduction in osmoregulatory work in an iso-osmotic environment.     

Effects of Stocking Density, Salinity, and Light Intensity on Growth and Survival of Southern Flounder Paralichthys lethostigma Larvae

Four separate studies were done on Southern flounder Paralichthys lethostigma larvae during first feeding and metamorphosis to determine the effects of stocking density, salinity, and light intensity on growth and survival. One study used stocking densities of 10, 20, 40, and 80 fish/L during first feeding; the second study compared the growth and survival of larvae stocked at 20 and 33 ppt; and a third experiment evaluated stocking densities of 1/L and 3/L under two different light intensities (1,600 lux vs 340 lux) during metamorphosis. The fourth experiment tested the effects of different salinities (0, 10, 20 and 30 ppt) on larval growth and survival during metamorphosis. Growth and survival (overall 6.9%) were not significantly different ( P > 0.05) for stocking rates up to 80/L. Larvae placed into 20 ppt salinity had survival through first feeding similar to that of larvae raised at 33 ppt. During metamorphosis, light intensity had no effect ( P > 0.05) on growth or survival, but fish stocked at 3/L had significantly lower ( P < 0.05) survival than fish at 1/L. Complete mortality of larvae occurred at 0 ppt. Growth and survival past metamorphosis were not significantly different ( P > 0.05) at 10, 20 and 30 ppt, but unmetamorphosed fish did not survive to day 60 at 10 ppt. Based on these results, practical larviculture of Southern flounder may require a two-step process with high stocking rates (80 fish/L) through first feeding and lower densities (1/L) through metamorphosis. Fingerling production in fertilized nursery ponds might he possible at salinity as low as 20 ppt.     

Effect of Low Salinity on Growth and Survival of Postlarvae and Juvenile Litopenaeus vannamei

The effect of low salinity on survival and growth of the Pacific white shrimp Litopenaeus vannamei was examined in the laboratory due to the interest of raising shrimp inland at low salinities. In three separate experiments, individual L. vannamei postlarvae (∼ 0.1 g) were cultured at salinities of either 0.5, 1, 1.5, 2, or 3 ppt ( N = 5 or 10/treatment) for 18 to 40 d at 30 C in individual 360-mL containers. In each experiment controls of 0 and 30 ppt were run. There was no postlarval survival at salinities < 2 ppt. Survival was significantly different ( P < 0.01) at 2 ppt (20%) compared to 30 ppt (80%). Growth was also significantly different ( P < 0.01) at 2 and 3 ppt compared to 30 ppt (416%, 475%, and 670%, respectively). A fourth experiment compared juveniles (∼ 8 g) and postlarvae (∼ 0.05 and 0.35 g). Shrimp were cultured at salinities of 0, 2, 4, and 30 ppt for 40 d at 25 C, in individual 360-mL and 6-L containers ( N = 7/treatment). There was no postlarval survival at < 2 ppt. Postlarval survival at 4 ppt (86%) was not significantly different (P > 0.05) from 30 ppt (100%). Juveniles exhibited better survival at lower salinities (100% at 2 ppt) than 0.05 and 0.35 g postlarvae (29% and 14% respectively, at 2 ppt). The effects of salinity on growth varied with sizdage. Final growth of 0.05 g postlarvae at 2 ppt (693%) was significantly less ( P < 0.01) than at 4 ppt (1085%) and 30 ppt (1064%). Growth of 0.35 g postlarvae was significantly less ( P < 0.01) for 4 ppt (175%) than for 30 ppt (264%). There was no growth data for juveniles (8 g). It appears from these experiments that the culture of L. vannamei poses risks when performed in salinities less than 2 ppt.     

Effects of manganese on juvenile mulloway (Argyrosomus japonicus) cultured in water with varying salinity—Implications for inland mariculture

The effects of 5 mg/L of dissolved manganese on juvenile mulloway at salinities of 5, 15 and 45 ppt were determined by comparing their survival, growth and blood plasma and organ chemistry with those of fish grown at the same salinities without manganese addition. Survival of mulloway at 45 ppt in the presence of 5 mg/L of manganese (73 ± 13%) was significantly lower than all other treatments, which achieved 100% survival. Those fish grown in water without manganese exhibited rapid growth, which was not affected by salinity (SGR = 4.05 ± 0.29%/day). Those fish grown at 5 ppt and 45 ppt in the presence of manganese lost weight over the 2-week trial (SGR − 0.17 ± 0.42 and − 0.44 ± 0.83%/day, respectively), whilst those at 15 ppt gained some weight (SGR 1.70 ± 0.20%/day). Manganese accumulated in the gills, liver and muscle of the fish and significant differences in blood plasma chemistry were observed. Blood plasma sodium and chloride of fish exposed to manganese were significantly elevated in hyperosmotic salinity (45 ppt) and depressed at hyposmotic salinity (5 ppt) compared with unexposed fish at the same salinity; consistent with manganese causing apoptosis or necrosis to chloride cells. We did not, however, observe any gill epithelial damage under light microscopy. Blood plasma potassium was significantly elevated at all salinities in the presence of manganese and liver potassium and glycogen reduced. These findings are consistent with manganese interfering with carbohydrate metabolism.     

Effects of different salinity and temperatures on the growth,survival, haematocrit and blood biochemistry of Goldfish (Carassius auratus)

The aim of the present study was to investigate the effects of different salinities (0‰, 6‰ and 12‰) and temperatures (23, 27 and 31 °C) on the food consumption, growth, blood biochemistry and haematocrit of Goldfish. After 45 days of exposure to different salinities and temperatures, Goldfish showed a good adaptation to these salinities and temperatures in terms of blood biochemistry (glucose and triglyceride) and haematocrit. Salinities (0‰ and 6‰) and temperatures (23 and 27 °C) did not affect the weight gain, specific growth rate, final biomass and feed conversion rates, but these parameters were significant (P<0.05) at 12‰ salinity and 31 °C temperature. Plasma total protein levels decreased with the increase in salinity (P<0.05), while they were independent of temperature. In conclusion, Carassius auratus, a freshwater stenohaline fish, showed good growth in saline waters with maximum 12‰ salinity and 31 °C temperature.     

Effects of Temperature and Salinity on Weight Gain, Oxygen Consumption Rate, and Growth Efficiency in Juvenile Red-Claw Crayfish Cherax quadricarinatus

Abstract.— Weight gain and metabolic rates, as determined by oxygen consumption rates, were examined in juvenile Australian red-claw crayfish Cherax quadricarinatus exposed to different temperatures (16–32 C in 2 C increments) or salinities (0–30 ppt in 5 ppt increments). Mean weight gain, molting frequency, and survival (%) were dependent on temperature and salinity. In freshwater (0 ppt), maximal weight gain and molting frequency were observed at 28 C with maximal survival observed over the temperature range of 24–30 C. Metabolic rates in freshwater were temperature dependent (mean Q₁₀= 2.44). Maximal weight gain and molting frequency were observed at salinities of 0 and 5 ppt (28 C); however, survival was reduced at salinities ≥ 5 ppt. Metabolic rates were not salinity dependent and did not differ significantly over the salinity range from 0–20 ppt. Growth efficiencies, calculated by dividing weight gain by total metabolic energy expenditure (i.e., weight gain + metabolic rate), were highest at a temperature of 20 C (0 ppt) and at salinities of 0 and 5 ppt (28 C). These data suggest that, at higher culture temperatures, maximal weight gain of red-claw juveniles may be reduced when food resources are limited. Maximal weight gain, at optimal temperatures (28 C) with unlimited food supply, does not appear to be effected by low salinity conditions. Because of the potential commercial value of red-claw, culturists, should be aware of the relationship between environmental condition and metabolic energy requirements to ensure maximal weight gain and survival of juveniles.     

Effect of Salinity on Larval Rearing of Pacu,Piaractus mesopotamicus,a Freshwater Species

The aim of this study was to evaluate the growth and survival of pacu, Piaractus mesopotamicus, larvae reared in different salinities and to determine the Artemia nauplii life span in freshwater and in saline water. First feeding 5‐d‐old pacu larvae were reared in freshwater or at 2, 4, 6, 8, 10, 12, and 14 ppt salinities. The larvae were reared in 1.5‐L aquaria at a density of 10 larvae/L with three replicates per treatment. After 10 d of rearing, significant differences (P < 0.05) were observed for growth and survival. Larval growth was higher at 2 and 4 ppt, and survival at 2 ppt was 100%. In freshwater and at 4, 6 and 8 ppt, the survival was 91.1, 93.3, 73.3, and 39.9%, respectively. At higher salinities, there was 100% mortality after 2 h (12 and 14 ppt) and 8 h (10 ppt) of exposure. The slightly saline water of at least 2 ppt increased the Artemia nauplii life span compared to the life span in freshwater. Later, in a second trial, 5‐d‐old pacu larvae were reared in freshwater and at 2 and 4 ppt salinities during the first 5 or 10 d of active feeding, and then the fish were transferred to freshwater. At the end of 15 d, larval growth was lower in freshwater (42 mg) than in treatments 2 and 4 ppt (59–63 mg). The abrupt transfer of fish from freshwater to slightly saline water and the return to freshwater did not affect the survival rates (89–97%). The larvae were able to adapt to these saline environments and handle abrupt changes in salt concentration. We concluded that salinity concentration of 2 ppt can be used for pacu larval rearing, allowing the Artemia nauplii lifetime to last longer and cause faster fish growth.     

Physiological short-term response to sudden salinity change in the Senegalese sole (Solea senegalensis)

The physiological responses of Senegalese sole to a sudden salinity change were investigated. The fish were first acclimated to an initial salinity of 37.5?ppt for 4?h. Then, one group was subjected to increased salinity (55?ppt) while another group was subjected to decreased salinity (5?ppt). The third group (control group) remained at 37.5?ppt. We measured the oxygen consumption rate, osmoregulatory (plasma osmolality, gill and kidney Na⁺,K⁺-ATPase activities) and stress (plasma cortisol and metabolites) parameters 0.5 and 3?h after transfer. Oxygen consumption at both salinities was higher than for the control at both sampling times. Gill Na⁺,K⁺-ATPase activity was significantly higher for the 55?ppt salinity at 0.5?h. Plasma osmolality decreased in the fish exposed to 5?ppt at the two sampling times but no changes were detected for high salinities. Plasma cortisol levels significantly increased at both salinities, although these values declined in the low-salinity group 3?h after transfer. Plasma glucose at 5?ppt salinity did not vary significantly at 0.5?h but decreased at 3?h, while lactate increased for both treatments at the first sampling time and returned to the control levels at 3?h. Overall, the physiological response of S. senegalensis was immediate and involved a rise in oxygen consumption and plasma cortisol values as well as greater metabolite mobilization at both salinities.     

Effects of Salinity on Growth, Survival, and Selected Hematological Parameters of Juvenile Cobia Rachycentron canadum

Cobia Rachycentron canadum juveniles (119.7 mm TL, weight 8.5 g) were reared for 10 wk at three salinity levels: 5 ppt, 15 ppt. and 30 ppt. Growth and survival were determined through biweekly sampling. Blood samples obtained at termination of the study were analyzed to determine hematocrit, blood osmolality, and total protein. Results indicated that the overall growth of fish was significantly affected by salinity. Mean (± SE) total length (TL) and weight of fish reared at a salinity of 30 ppt were 201.7 ± 2.6 mm and 47.6 ± 1.9 g, respectively, followed by fish reared at 15 ppt (182.2 ± 1.7 mm, 34.1 ± 1.6 g). and 5 ppt (168.3 ± 5.8 mm TL, 28.3 ± 2.3 g). Differences in specific growth rates among treatments for the 10-wk period were also significant. No differences were detected in mean survival among fish reared at salinities of 5, 15, and 30 ppt (84, 94, and 94%, respectively). However, fish reared at salinity 5 ppt appeared to be in poor health as skin lesions, fin erosion, and discoloration were evident. Analysis of blood revealed that, while no differences existed among treatments with respect to plasma total protein, fish reared at a salinity of 5 ppt exhibited significantly reduced hematocrit (25% vs. > 30%) and plasma osmolality values (318 vs. > 353 mmolkg) relative to fish reared at higher salinities. Cobia can tolerate exposure to low salinity environments for short periods of time without mortality; however, moderate to high salinities are required for sustained growth and health of this species.     

Salinity During Early Development Influences Growth and Survival of Florida Red Tilapia in Brackish and Seawater

Growth of juvenile Florida red tilapin (1.57 g average weight) spawned and sex-reversed (monosex male) at salinities of 4 ppt and 18 ppt was compared at rearing salinities of 18 ppt and 36 ppt in 200 L aquaria under controlled photoperiod (12 L:12 D) and temperature (28 C). Growth was significantly higher for progeny spawned at 18 ppt than those spawned at 4 ppt under both rearing salinities with no difference observed between 18 ppt and 36 ppt.
In another experiment, growth of juvenile progeny (0.98 g average weight) spawned and sex-reversed at salinities of 2 ppt and 18 ppt was compared in 24 m³ outdoor pools at 36 ppt. When water temperatures exceeded 27 C, growth and survival were not significantly different between these groups. However, when temperatures fell below 25 C, growth and survival were significantly higher among progeny spawned at 18 ppt.
The results showed that progeny spawned and reared through early ontqenetic development in brackishwater are better adapted for growth in brackish and seawater and suggested that these fish may have higher resistance to cold-stress in seawater than progeny spawned in freshwater.     

Growth of Stocker Channel Catfish to Large Market Size in Single-Batch Culture

Catfish farmers increasingly are producing fish larger than the traditional size of 0.45-0.57 kg/fish in order to meet processing plant requirements for larger fish. Production of larger channel catfish Ictalurus punctatus in multiple-batch culture has been investigated in a few studies, but the impact of understocked fingerlings on growth of carry-over fish is unknown. The present study was conducted to quantify growth, feed conversion ratio, net daily yield, and net and total yield of stocker channel catfish grown in single-batch, one-season culture to mean individual weights of 0.60, 0.72, 0.91, or 1.17 kg/fish. Channel catfish (mean weight = 0.26 kg/fish) were stocked into 12 0.1-ha ponds at 11,115 fish/ha. Fish were fed a 32% crude protein floating extruded feed once daily to apparent satiation. When the average weight of the fish population reached the target weight, three randomly selected ponds were harvested. Fish growth was linear in all treatments. Growth rates were similar for fish grown to 0.60, 0.72, and 0.91 kg/fish, and significantly lower ( P < 0.05) than for fish grown to 1.17 kg. Variation in individual fish weight increased linearly with increased duration of culture period. Feed conversion ratio averaged 1.9 and did not differ significantly among treatments. The percentage of the fish population at harvest that fell within the 0.57 to 2.04 kg-size range preferred by processing plants increased from 56.6 to 98-5% as the mean weight at harvest increased from 0.60 to 1.17 kg/fish.     

Temperature and Salinity Tolerances of the Tropical Spiny Lobster,Panulirus ornatus

Interest in the development of aquaculture of the tropical spiny lobster, Panulirus ornatus, has increased markedly over the past 10 yr because of strong market demand and high prices. In Australia, economic conditions will necessitate that a semi‐intensive approach be taken, possibly involving managed environmental conditions. Identification of optimal temperature and salinity levels will be necessary, and therefore two experiments were performed to examine these two parameters. Juvenile lobsters were grown in tanks at five temperatures (19, 22, 25, 28 and 31 C). Growth was significantly affected by temperature (P < 0.01), and maximal growth occurred at 25–31 C. Examination of the temperature effect on molt increment and intermolt period indicated that 27 C was the optimal temperature, at which molt increment was greatest and intermolt period the least. Temperature also had a significant (P < 0.01) positive effect on apparent feed intake (AFI). Juvenile lobsters were also exposed to four different salinities (20, 25, 30 and 35 ppt) over a period of 91 d. Significant differences (P < 0.01) were apparent for both survival and growth. Lowest survival occurred at 35 ppt which may be attributable to higher cannibalism at that salinity. Growth was highest at 35 ppt and progressively less at lower salinities. Although full marine salinity (35 ppt) will generate best performance of P. ornatus, its capacity to tolerate reduced salinity will provide greater opportunity to develop commercial aquaculture.     

Evaluation of duckweed (Lemna gibba) as feed for tilapia (Oreochromis niloticus × O. aureus) in a recirculating unit

Hybrid Oreochromis niloticus × O. aureus were cultured at high densities in an experimental recirculating unit over a period of 89 days with duckweed (Lemna gibba) or a combination of duckweed and commercial pellets as feed. When fed duckweed alone, intake rate was low, feed conversion ratio good (1:1) and relative growth rate poor (0.67% of body mass d^?1). Sixty five percent of the duckweed consumed was assimilated and 26% converted to fish. When the fish were fed pellets in addition to duckweed the rate of duckweed consumption decreased and growth rate of the fish doubled with feed conversion ratios between 1.2 and 1.8. Seventy percent of the mixed diet was assimilated but only 21% converted. Fish grown on the mixed diet performed similarly to fish grown on pellets but had a better feed conversion ratio.     

豆粕型饲料中添加蛋氨酸对江黄颡鱼生长的影响

研究了在豆粕型饲料中添加不同浓度的蛋氨酸对江黄颡鱼生长的影响。试验鱼分为3个组,蛋氨酸的添加量分别为0、0.2%、0.4%,分别对应Ⅰ、Ⅱ、Ⅲ组,Ⅰ组设为对照组,饲养周期为8周。试验结果表明,Ⅱ组、Ⅲ组的质量增长率显著高于对照组(P<0.05),其中Ⅱ组质量增长率最高(176.22±3.56)%;Ⅱ组的成活率显著高于对照组(P<0.05);各组的饲料系数与对照组比较无显著性差异(P>0.05),Ⅲ组饲料系数最小(2.60±0.13);各试验组之间的摄食量差异不显著(P>0.05),Ⅱ组的摄食量较对照组高12.50%。在本研究条件下,建议蛋氨酸的添加量为0.2%~0.4%。     

Effect of Water Temperature on Growth, Survival, and Biochemical Composition of Largemouth Bass Micropterus salmoides

The effects of water temperature on growth rate, survival, and biochemical composition of juvenile largemouth bass Micropterus salmoides were evaluated under controlled conditions in tanks for 12 wk. Feed-trained juvenile largemouth (9.1 ± 1.9 g) were stocked into nine 3,610-L polyethylene tanks inside a greenhouse structure at 140 fish/m³ (500 fish/tank). Three treatment temperatures were evaluated (20, 26, and 32 C) with three replicates per treatment. Bass were fed to apparent satiation twice daily using a commercially available floating salmonid diet (45% crude protein and 16% lipid). After 97 d bass grown at 26 and 32 C had significantly higher ( P < 0.05) average weights, SGR, condition factor (K), and production rates (kg/m³) than those in the 20 C treatment. Bass in the 26 C treatment had significantly lower ( P 0.05) FCR and higher percent protein deposit (PPD) than bass raised at 20 and 32 C, which were not significantly different ( P >0.05). There were no significant differences ( P >0.05) in survival among treatments which averaged 97%, overall. Bass raised at 32 C had higher ( P 0.05) lipid levels in the liver than other treatments. Whole body amino acid concentrations were not significantly impacted ( P >0.05) by culture temperature. Largemouth bass raised at 26 C had significantly lower ( P 0.05) levels of stearic acid (18:0) and significantly higher ( P 0.05) levels of arachidonic acid (20:4 n-6) than bass raised at 20 or 32 C. Bass raised at 32 C had significantly higher ( P 0.05) levels of Linoleic acid (18:2 n-6), total saturates, and dienes than bass raised at 26 or 20 C. These data indicate that growth and feed conversion efficiency are reduced at 20 C. Growth is similar at 26 and 32 C, but feed and dietary protein are more efficiently utilized at 26 C.