The Effects of Temperature, Age, and Acclimation to Salinity on the Survival of Farfantepenaeus paulensis Postlarvae

Abstract.— Salinity tolerance limits during the ontogenetic development of Farfantepenaeus paulensis postlarvae (PL) were determined at different temperatures. Initially, PL 10, 20, 30, 40, 60 and 80 maintained in 30 ppt (parts per thousand) salinity, 22‐25 C, were directly transferred to 15 combinations of salinity (2, 5, 10, 20 and 30 ppt) and temperature (15, 20 and 30 C) for 96 h. Irrespective of age or salinity, higher survival rates were registered at 25 C. PL 10 suffered high mortality, especially at low salinities combined with low (15 C) or high (30 C) temperatures. From PL 20 to PL 40, an increase in survival was observed in all combinations. For PL 60 and 80, tolerance to low salinity was reduced, suggesting that PL have a maximum age by which they are able to develop adaptability to low salinities. In general, the effect of temperature contributed more significantly to mortality in PL 10 and PL 30, but its influence decreased afterwards. From PL 40, salinity becomes the main factor determining mortality. In order to examine the effects of acclimation to salinity on the tolerance limits, a second set of experiments was performed with PL 5, 10, 15 and 25 acclimated to 2, 5, 10, 20 and 30 ppt, 25 C, over a 5‐d period. Postlarvae were then transferred to different salinity levels (2, 5, 10, 20 and 30 ppt) and kept for 96 h. High mortality of PL 10 occurred after direct transfer from high to intermediate/low salinity levels. Although the acclimation to salinity increased survival, it was still poor. An increase in the salinity tolerance was observed from PL 15 to 30, even with no acclimation. Results indicate that PL 10 do not have a fully developed osmoregulatory capacity to cope with low and/or abrupt changes of salinity. It is recommended that non‐acclimated PL 10 should only be released in environments with salinity at or above 20 ppt. If acclimation is carried out, PL may be released in salinities above 10 ppt. The release of PL 10 in salinities below 5 ppt may result in mortality rates of up to 70%. The best age for the release of non‐acclimated F. paulensis PL in environments with low and/ or wide fluctuations of salinity would he PL 15‐30.     

Effect of Salinity on Hatching in Neobenedenia melleni, a Monogenean Ectoparasite of Seawater-Cultured Tilapia

Laboratory experiments were conducted to determine the effect of salinity on embryonic development and hatching in Neobenedenia melleni , a monogenean ectoparasite of seawater-cultured (37 ppt) Florida red tilapia ( Oreochromis urolepis hornorum × O. mossambicus ). Eggs, collected from adult monogeneans at 37 ppt, were exposed to different salinities (0, 6, 12, 18, 24, 30 and 37 ppt) for 48, 72 or 96 h. Varying degrees of post-treatment development and hatching occurred when natural seawater conditions were restored. Hatching success generally declined with decreasing salinity and increasing duration of exposure. Under all durations of exposure, hatching success remained relatively high (≥ 69.6%) at salinities of 24 ppt and above, but declined markedly (≤ 32.5%) at lower salinities. Hatching did not occur in eggs exposed to fresh water (0 ppt) for 72 and 96 h. The most effective treatments in preventing hatching, other than prolonged exposure to fresh water, were 96 h exposures to low-salinity brackish water. Percent hatch after 96 h exposure to 6, 12 and 18 ppt was 5.5, 11.9 and 5.8%, respectively.     

Acute Toxicity and Anesthetic Effects of Clove Oil in Penaeus semisulcatus under Various Water Quality Conditions

Acute toxicity and anesthetic effects of clove oil were studied in P. semisulcatus (1.8–2.1 g body weight). The EC₅₀ 1-h (the concentration effective for 50% of test animals), LC₅₀ 1-h (the concentration lethal to 50% of test animals after 1 h) and LC₅₀ 24-h (the concentration lethal to 50% of test animals after 24 h) were calculated at concentrations of 25, 130 and 30 mg/l, respectively, at 30°C, salinity 40 ppt, pH 8.6 and dissolved oxygen >6 mg/l. Generally, with increasing concentrations of clove oil, the times required for sedation and anesthesia decreased, while the recovery times increased. At concentrations 50, 100, 150 and 200 mg/l under temperature of 30°C and salinity of 40 ppt, the times required for sedation were 6 ± 0.2, 2.5 ± 0.3, 2 ± 0.08 and 0.5 ± 0.08 min, while times required for complete recovery were calculated to be 4.5 ± 0.3, 5.5 ± 0.17, 6.5 ± 0.25 and 11 ± 0.38 min, respectively. Also, the times required for deep anesthesia were 20 ± 1, 5 ± 0.5, 3 ± 0.4 and 2.2 ± 0.5 min in the above concentrations, while the times required for complete recovery were 10 ± 1, 11 ± 1.5, 14 ± 2.2 and 16 ± 3 min, respectively. Furthermore, considering the times to sedation, deep anesthesia and recovery at different temperatures of 20°C, 25°C, 30°C and 35°C and salinities of 25, 30, 35, 40 and 48 ppt; the combinations of salinity plus temperature and clove oil concentration plus salinity had the greatest and the least effects.     

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.     

Size dependent early salinity tolerance in two sizes of juvenile white sturgeon,Acipenser transmontanus

The objective of this study was to investigate the influence of size on salinity tolerance in 1 year old juvenile white sturgeon. Two sizes of sturgeon (10 and 30 g) from the same spawning event (thus reducing confounding effects of genetic make-up and size) and reared in the same environment were exposed to a salinity of 0, 8, 16, 24, or 32 ppt for up to 120 h. Both 10 and 30 g fish exhibited > 93% mortality within 24 h after transfer to 24 or 32 ppt, regardless of whether they were transferred directly from freshwater (FW) or following a 48 h pre-treatment period at 16 ppt. Direct transfer from FW to 16 ppt was associated with 25 to 30% mortality, indicating that these fish have some ability to tolerate large changes in salinity for up to 5 days at this stage. Following exposure to 8 and 16 ppt, an elevation in plasma osmolarity, [Na⁺], and [Cl^?] was observed between 24 and 72 h in both 10 and 30 g sturgeon, but plasma ions and osmolarity in surviving fish at 120 h were not significantly different between groups held at 0, 8, and 16 ppt. Despite being unprepared for either direct or stepwise transfer to salinities of 24 ppt or greater, size confers some ionoregulatory advantage, as mortality occurred more slowly and the degree of ionoregulatory perturbation was less in 30 g than 10 g fish over the course of the exposures. It is not known whether the apparent advantage of size is related to a size-dependent development of ionoregulatory capacity or due to social status which can also influence ionoregulatory capacity, but age and genetic differences did not likely contribute to this size effect.     

Acute Toxicity of Ammonia and Nitrite to Sea Bream,Sparus aurata (Linnaeus, 1758), in Relation to Salinity

Sea bream, Sparus aurata, is one of the most important fish species that is commonly cultured in the Mediterranean and the eastern coasts of the Atlantic Ocean. The life cycle of sea bream in its natural habitat passes through hyposaline and hypersaline lagoons. It is important to determine the tolerance of the fish to nitrogenous compounds for aquaculture at maximum stocking densities. In the present study, a series of acute experiments were performed to evaluate the effect of salinity on ammonia and nitrite toxicity to sea bream. The fish were exposed to different ammonia and nitrite concentrations according to the static renewal methodology at three different salinities (10, 20, and 30 ppt) and at a temperature of 20 C and a pH of 8.2. The toxic effect of total ammonia nitrogen (TAN) and nitrite nitrogen (NO₂‐N) decreased with increasing salinity levels (P < 0.001). Acute toxicity (96‐h lethal concentration 50 [LC₅₀]) values of TAN were determined to be 5.93, 11.72, and 19.38 mg/L at 10, 20, and 30 ppt salinity, respectively. The 96‐h LC₅₀ values of NO₂‐N were determined to be 370.80, 619.47, and 806.33 mg/L at 10, 20, and 30 ppt salinity, respectively. Results indicate that sea bream is less tolerant to ammonia but more tolerant to nitrite compared with some other fish species.     

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.     

Acute tolerance of juvenile Florida pompano, Trachinotus carolinus L., to ammonia and nitrite at various salinities

The acute tolerance of juvenile Florida pompano Trachinotus carolinus L. (mean weight±SE=8.1±0.5 g) to environmental unionized ammonia‐nitrogen (NH₃‐N) and nitrite‐nitrogen (NO₂‐N) at various salinities was determined via a series of static exposure trials. Median‐lethal concentrations (LC₅₀ values) of NH₃‐N and NO₂‐N at 24, 48, and 96 h of exposure were calculated at salinities of 6.3, 12.5 and 25.0 g L^?1 at 28 °C (pH=8.23–8.36). Tolerance of pompano to acute NH₃‐N exposure was not affected by salinity, with 24, 48 and 96 h LC₅₀ values ranging from 1.05 to 1.12, 1.00 to 1.08 and 0.95 to 1.01 mg NH₃‐N L^?1 respectively. Regarding NO₂‐N, tolerance of pompano to this environmental toxicant was compromised at reduced salinities. Median‐lethal concentrations of NO₂‐N to pompano at 24, 48 and 96 h of exposure ranged from 67.4 to 220.1, 56.9 to 140.7 and 16.7 to 34.2 mg NO₂‐N L^?1 respectively. The results of this study indicate that juvenile Florida pompano are relatively sensitive to acute NH₃‐N and NO₂‐N exposure, and in the case of the latter, especially at lower salinities.     

Changes in Na+,K+-ATPase activity and gill chloride cell morphology in the grouper Epinephelus coioides larvae and juveniles in response to salinity and temperature

The activity of the enzyme Na⁺,K⁺-ATPase and morphological changes of gill chloride cells in grouper, Epinephelus coioides larvae and juveniles were determined 6–48 h after abrupt transfer from ambient rearing conditions (30–32 ppt, 26.5–30 °C) to different salinity (8, 18, 32, 40 ppt) and temperature (25, 30 °C) combinations. Na⁺,K⁺-ATPase activity in day 20 larvae did not change at salinities 8–32 ppt. Activity decreased significantly (P <0.01) after exposure to 40 ppt at 25–30 °C, which was accompanied by an increase (P <0.05) in density and fractional area of chloride cells. Enzyme activity in 40 ppt did not reach a stable level and larvae failed to recover from an osmotic imbalance that produced a low survival at 25 °C and death of all larvae at 30 °C. Enzyme activity and chloride cell morphology in day 40 groupers did not change in 8–40 ppt at 25 °C and 8–32 ppt at 30 °C. A significant decrease and a subsequent increase in Na⁺,K⁺-ATPase activity in 40 ppt at 30 °C was associated with the increase in chloride cell density resulting in an increased fractional area but a decreased cell size. Enzyme activity and chloride cells of day 60 grouper were unaffected by abrupt transfer to test salinities and temperatures. These results demonstrate that grouper larvae and juveniles are efficient osmoregulators over a wide range of salinities. Salinity adaptation showed an ontogenetic shift as the larvae grew and reached the juvenile stage. This development of tolerance limits may reflect their response to actual conditions existing in the natural environment.     

盐度对俄罗斯鲟幼鱼血清渗透压、离子含量及鳃丝 Na+/K+-ATP 酶活力的影响

研究了急性盐度胁迫对7月龄俄罗斯鲟(Acipenser gueldenstaedtii)幼鱼[体质量(86.1±18)g]鳃丝Na+/K+-ATP酶活力、血清渗透压和血清离子(Na+、K+、Cl-)的影响。结果表明:幼鱼从淡水直接转入盐度15、20、25水中,96h死亡率分别为72.22%、100%、100%,其他组(盐度0、5、10)无死亡。各盐度组96h血清渗透压、Na+、Cl-浓度随盐度升高而增加,且各盐度组显著高于对照组(P0.05),盐度15组最高,盐度5、10组间各指标不存在显著差异(P0.05)。盐度组血清K+离子在48h中较对照组均显著降低(P0.05),96h时有所回升但仍低于对照组,盐度15与盐度5、10相比血清K+离子有显著性差异(P0.05),盐度5、10之间无显著性差异(P0.05)。盐度组鳃丝Na+/K+-ATP酶活力呈先下降后上升变化,48h为最低,与对照组有显著性差异(P0.05),96h时盐度5、10组鳃丝Na+/K+-ATP酶活力与对照组及组间无显著差异(P0.05),盐度15与对照组及盐度5、10均有显著差异(P0.05)。96h幼鱼的等渗点为303.2mOsm·kg-1,相当于盐度10.06,而Na+及Cl-等离子点分别为146.1mmol·L-1和136.8mmol·L-1,分别相当于盐度9.02和8.95。与盐度15组相比,盐度10及其以下处理组各项检测指标变化幅度相对较小,在幼鱼渗透调节范围之内,盐度10中养殖15d后各项指标与淡水组差异较小,因此7月龄俄罗斯鲟幼鱼已具备在盐度10及以下的咸水中生活的能力,但不能耐受高于10的盐度。     

PRELIMINARY EVALUATION OF SURVIVAL AND GROWTH OF JUVENILE RED DRUM (Sciaenops ocellata) IN FRESH AND SALT WATER

Heretofore few quantitative studies on the tolerance of red drum (Sciaenops ocellata Linnaeus) to freshwater (FW) or dilute sea water have been conducted. In the laboratory we subjected larval and juvenile stages of red drum to dechlorinated FW for 96 hours and found 5% survival in larvae (23-day-old, 6.2 mm SL), 70% for postlarvae (34 and 47-day-old, 16.2 mm to 19.7 mm SL) and 95% for juveniles (57-day-old, 56.9 mm SL). Survival in control salinities of 10 ppt was 90% or greater. The results indicate that tolerance to dilute media is size dependent. In a separate experiment growth of juvenile red drum (52 mm SL) over a 30-day period was compared in two raceways with flow-through supplies of dechlorinated FW, and SW of ambient (35±2 ppt) salinity. SW fish grew significantly larger (P < .01) than those acclimated to FW. Within both treatments a large size differential developed with time. Food conversion efficiency was improved and appetite drive was enhanced in the SW treatment. Percent survival after 30 days was comparably high (93%) in both treatments. Fast growth and high survival of juvenile (>20 mm SL) red drum promote the feasibility of this valuable sport and commercial species in both FW and SW aquaculture. Its potential as a control fish in FW fishery management deserves further investigation.     

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 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.     

The Effects of Temperature and Salinity on Early Life Stages of Black Sea Bass Centropristis striata

Along the Atlantic coast black sea bass occur from the Gulf of Maine to Florida and support important commercial and recreational fisheries. Interest in commercial production of black sea bass has increased in recent years due to high demand and limited seasonable availability. Efforts towards large-scale production have been hampered by a high incidence of early larval mortality. Two of the most important environmental variables affecting hatchery production of marine finfish larvae are temperature and salinity. In the wild, larval black sea bass are found in waters with temperatures of 12–24 C and salinity levels of 30–35 ppt. Studies were conducted to define the temperature and salinity ranges that support growth and development of black sea bass during early life stages. Three developmental phases were investigated: 1) fertilization to hatch: 2) hatch through yolk sac absorption: and 3) during the initial exogenous feeding stage (5–14 days post hatch: DPH). Fertilized eggs were obtained by manual spawning of fish following administration of LHRH_a. Fertilized eggs were transferred to 300-mL glass Petri dishes or 500-mL beakers to assess the effects of salinity and temperature through hatch and yolk sac absorption, respectively. To determine environmental effects on growth and survival during initial exogenous feeding 400 actively feeding larvae were cultured in green water and fed enriched rotifers for a 9-d period. For investigation of the effect of salinity, sea water (35 ppt) was diluted gradually to 15, 20, 25, and 30 ppt and maintained at 21 C. For examination of the effect of temperature, seawater was adjusted from 21 C to 12, 15, 21, 27, or 30 C at a rate of 3 C/h. No eggs hatched at 12 C or when salinity was maintained at 0 or 5 ppt. Hatching was uniformly high (≥ 85%) at temperatures between 15 and 27 C and at salinities ≥ 15 ppt. Survival through yolk sac absorption was greatest at temperatures between 18 and 27 C and at salinities ≥ 20 ppt. Survival through first feeding stage was highest at temperatures ≥ 18 C and 30 ppt salinity. Larval growth through first feeding was not significantly affected by salinity level but did increase with rearing temperature. The results indicate that survival and development of black sea bass during early life stages are most favorable at temperatures >18 C with salinity levels approaching full strength seawater.     

Salinity tolerance of Nile tilapia fry (Oreochromis niloticus), spawned and hatched at various salinities

Fertilized eggs of the Nile tilapia (Oreochromis niloticus L.) spawned in freshwater, were removed from mouthbrooding females, 1 day post-spawning and artificially incubated at elevated salinities. At 6 days post-hatching, mean survivals of 85.5, 84.4, 82.5, 56.3, 37.9, 20.0 and 0% were recorded for broods incubated at salinities of 0, 5, 10, 15, 20, 25 and 32 ppt, respectively. Fertilized eggs exhibited a 96-h median lethal salinity (MLS-96) of 18.9 ppt, a value identical to that of 7- to 120-day-old fry and fingerlings. Fertilized eggs exhibited a higher median survival time (ST₅₀ = 978 min) than 7- to 395-day-old fry and fingerlings (ST₅₀ = 28.8–179.0 min).The salinity tolerances of fry spawned at various salinities and fry spawned in freshwater but hatched at various salinities, were determined using the median survival time (ST₅₀), mean survival time (MST) and 96 h-median lethal salinity (MLS-96) indices. For comparative purposes, fry spawned and hatched in freshwater were acclimatized to various salinities and their salinity tolerance determined. Fry salinity tolerance progressively increased with increasing salinity of spawning, hatching, or acclimatization. However, at equivalent salinity, early exposure (spawning) produced progeny of comparatively higher salinity tolerance than those spawned in freshwater and hatched at elevated salinity. Similarly, at equivalent salinity, progeny spawned in freshwater but hatched at elevated salinity exhibited higher salinity tolerance than those spawned and hatched in freshwater, then acclimatized to an elevated salinity.The utility of these methods of early salinity exposure toward the saltwater culture of tilapias is discussed.     

Effects of Salinity on Growth and Energy Budget of Juvenile Cobia,Rachycentron canadum

The effects of salinity on the growth and energy budget of juvenile cobia, Rachycentron canadum, were evaluated. Triplicate tanks with ten fish per tank (initial weight 17.58 ± 0.26 g/fish, mean ± SD) reared at salinities of 5, 10, 15, 20, 25, 30, and 35 ppt were fed with fresh squid to satiety for 15 d. Results indicated that there were no significant differences in daily ration level in wet weight (RL_w), dry weight (RL_d), and energy (RL_e) of the fish. There were also no significant variations in daily fecal production (f_e) and apparent digestibility coefficient of energy (ADC_e) among salinity treatments. Specific growth rates (SGRs) in wet weight (SGR_w), dry weight (SGR_d), and energy (SGR_e) showed domed curves relative to salinity. Quadratic regression analyses of SGR_w, SGR_d, and SGR_e against salinity indicated that the optimal salinity for maximal growth of juvenile cobia was 29.9, 29.9, and 28.5 ppt, respectively. Similar to the trend of SGR, food conversion efficiency for juvenile cobia in wet weight (FCE_w), dry weight (FCE_d), and energy (FCE_e) increased with the increases in salinity, maximized at 30 ppt, and then decreased when salinity reached 35 ppt.     

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.     

Larval growth, survival and development of Metapenaeus monoceros (Fabricius) cultured in different salinities

Larvae of Metapenaeus monoceros (Fabricius) at protozoea 1 (PZ1) stage were stocked in 2‐L glass flasks to investigate the effects of various salinities (25, 30, 35, 40, 45, 50 and 55 ppt) on growth and survival until the post‐larval (PL) stages. The PZ larvae were not able to tolerate a sudden salinity drop of over 10 ppt. Yet, an abrupt salinity increase of over 10 or even 15 ppt did not cause mortality. The PZ larvae were successfully acclimated to different test salinities at a rate of 4 ppt h^?1. The larvae displayed better tolerance to high rather than low salinities. The lowest and highest critical salinities appeared to be 22 and 55 ppt respectively. Taking into account survival, growth and development results, the optimal salinity for the larval culture of M. monoceros inhabiting the Eastern Mediterranean was 40 ppt. At this salinity, the PZ1 larvae were successfully cultured until PL1 stage within 11 days with 68% survival on a feeding regime of Tetraselmis chuii Kylin (Butcher) (20 cells μ L^?1), Chaetoceros calcitrans Paulsen (50 cells μ L^?1), Isochrysis galbana Parke (30 cells μL^?1) and five newly hatched Artemia nauplii mL^?1 from M1 onwards at 28 °C.     

Survival of Post‐larval Litopenaeus vannamei Following Acclimation to Low Salinity Waters at Different Temperatures

Temperature and salinity are two factors known to influence the growth potential and survival of the Pacific white shrimp, Litopenaeus vannamei, acclimated to low salinity waters. In west Alabama, farmers suspect low water temperatures at stocking, in conjunction with low salinity and suboptimal ionic profiles, might be responsible for reduced survival and production at harvest. To determine the influence of temperature and salinity on post‐larval (PL) L. vannamei, a series of bioassays were conducted at the E.W. Shell Fisheries Research Station in Auburn, Alabama and Claude Peteet Mariculture Center in Gulf Shores, Alabama. PL L. vannamei of ages 11, 13, and 20 (PL₁₁, PL₁₃, and PL₂₀) were acclimated down to salinities of 12, 4, 2, 1, 0.5, and 0.2 ppt at different temperatures ranging from 17.6 to 24.0 C. During the acclimation bioassays survivals were assessed at 24 and 48 h. PL survival of the three age groups examined were significantly reduced at salinities of 1, 0.5, and 0.2 ppt. These results correspond well to those reported at higher temperatures confirming that across the tested temperature range salinity endpoint was the driving factor in determining survival and that suboptimal temperatures had a minimal influence on survival.     

Effect of salinity on survival, growth, oxygen consumption and ammonia-N excretion of juvenile whiteleg shrimp, Litopenaeus vannamei

In this study, we tested the lower salinity tolerance of juvenile shrimps (Litopenaeus vannamei) at a relatively low temperature (20 °C). In the first of two laboratory experiments, we first abruptly transferred shrimps (6.91 ± 0.05 g wet weight, mean ± SE) from the rearing salinity (35 000 mg L^?1) to salinities of 5000, 15 000, 25 000, 35 000 (control) and 40 000 mg L^?1 at 20 °C. The survival of L. vannamei juvenile was not affected by salinities from 15 000 to 40 000 mg L^?1 during the 96‐h exposure periods. Shrimps exposed to 5000 mg L^?1 were significantly affected by salinity, with a survival of 12.5% after 96 h. The 24‐, 48‐ and 96‐h lethal salinity for 50% (LS₅₀) were 7020, 8510 and 9540 mg L^?1 respectively. In the second experiment, shrimps (5.47 ± 0.09 g wet weight, mean ± SE) were acclimatized to the different salinity levels (5000, 15 000, 25 000, 35 000 and 40 000 mg L^?1) and then maintained for 30 days at 20 °C. Results showed that the survival was significantly lower at 5000 mg L^?1 than at other salinity levels, but the final wet weight under 5000 mg L^?1 treatment was significantly higher than those under other treatments (P<0.05). Feed intake (FI) of shrimp under 5000 mg L^?1 was significantly lower than those of shrimp under 150 00–40 000 mg L^?1; food conversion efficiency (FCE), however, showed a contrasting change (P<0.05). Furthermore, salinity significantly influenced the oxygen consumption rates, ammonia‐N excretion rates and the O/N ratio of test shrimps (P<0.05). The results obtained in our work provide evidence that L. vannamei juveniles have limited capacity to tolerate salinities <10 000 mg L^?1 at a relatively low temperature (20 °C). Results also show that L. vannamei juvenile can recover from the abrupt salinity change between 15 000 and 40 000 mg L^?1 within 24 h.