Growth of juvenile common snook (Centropomus undecimalis Bloch, 1792) reared at different temperatures and salinities: Morphometric parameters,RNA/DNA,and protein/DNA ratios

We investigated the growth of juvenile common snook (Centropomus undecimalis) reared at 25°C and 28°C and salinities of 0.3, 15, and 32 g L^?1. Total length, weight, RNA/DNA, and protein/DNA ratios were determined after 90 days of experiment. Higher growth was observed at 28ºC compared with 25°C, at the same salinity. At 28°C and 15 g L^?1 salinity, the weight (25.14 g) of juveniles was twice that of the juveniles reared at the lower temperature. At different salinities, only higher temperature affected growth, with higher weight values obtained at 15 g L^?1 in comparison with 0.3 and 32 g L^?1. Length was similar at 0.3 and 15 g L^?1. The RNA/DNA ratio was greater in juveniles reared at a salinity of 15 g L^?1 when compared with 0.3 and 32 g L^?1. This study shows that the combination of higher temperature and intermediate salinity promotes better growth of common snook juveniles.     

Effect of low salinity on microbial floc composition and performance of Litopenaeus vannamei (Boone) juveniles reared in a zero‐water‐exchange super‐intensive system

This study aimed to evaluate the effect of low salinity on the water quality, microbial flocs composition and performance of Litopenaeus vannamei juveniles reared over 40 days in a zero‐water‐exchange super‐intensive system at 0, 2, 4 and 25 g L^?1. At 0 g L^?1, the mortality was total at the 26th day, and consequently, these salinity data were not included in the statistical analysis. Among the water quality parameters, only pH and the total suspended solids concentration were significantly influenced by salinity. However, a trend towards intensification of the nitrification processes was observed as the salinity increased, with the lowest ammonia and the highest nitrite and nitrate concentrations found at 25 g L^?1. The concentrations of ciliates and flagellates diminished and increased, respectively, with the increase in salinity. Diatoms predominated at 25 g L^?1, whereas at 2 and 4 g L^?1, chlorophytes were more abundant. Microbial floc crude protein content was reduced with the increase in salinity, whereas ash content demonstrated the inverse trend. The best overall growth performance and survival were observed at 25 g L^?1. However, satisfactory productivity was also found at 4 g L^?1, suggesting the viability of rearing L. vannamei at low salinity under zero‐water‐exchange conditions.     

Effect of hypo- and hyper-saline conditions on osmolarity and fatty acid composition of juvenile shrimp Litopenaeus vannamei (Boone, 1931) fed low- and high-HUFA diets

Litopenaeus vannamei (Boone) grown in ponds are exposed to salinities of less than 5 g L^?1 during inland shrimp culture or to more than 40 g L^?1 from evaporation and reduced water exchange in dry, hot climates. However, dietary requirements for shrimp grown in low or high salinities are not well defined, particularly for fatty acids. Feeding shrimp postlarvae with highly unsaturated fatty acids (HUFA) enhances tolerance to acute exposure to low salinity, as a result of better nutritional status, or/and specific effects of HUFA on membrane function and osmoregulation mechanisms. This study analysed the effect of HUFA supplementation (3% vs. 34%) on L. vannamei juveniles reared for 21 days at low (5 g L^?1), medium (30 g L^?1) and high salinities (50 g L^?1). Juveniles grown at 5 g L^?1 had lower survival compared with controls (30 g L^?1) or shrimp grown at 50 g L^?1, but no significant effect on survival was observed as a result of HUFA enrichment. In contrast, growth was significantly lower for shrimp grown at 50 g L^?1, but this effect was compensated by the HUFA‐enriched diet. Osmotic pressure in haemolymph was affected by salinity, but not by HUFA enrichment. Shrimp fed HUFA‐enriched diets had significantly higher levels of eicosapentaenoic acid and docosahexaenoic acid in hepatopancreas and gills. These results demonstrate that growth at high salinities is enhanced with diets containing high HUFA levels, but that HUFA‐enriched diets have no effect on shrimp reared at low salinities.     

Evaluation of resistance to Dermo in eastern oyster strains tested in Chesapeake Bay

We investigated growth, Dermo disease, and survival for nine groups of oysters, Crassostrea virginica (Gmelin) cultivated in Chesapeake Bay (CB). Five regional strains (upper CB, North Carolina (NC), South Carolina (SC), Louisiana (LA) and LA triploids) and four additional hybrid strains (CB oysters mated with NC, SC, LA and Texas (TX) oysters) were held in floating rafts at three locations representative of lower CB: ‘low’ salinity (3–14 g L^?1), ‘moderate’ salinity (5–20 g L^?1) and ‘high’ salinity (14–24 g L^?1). At each site, patterns of growth and incidence of infection with Perkinsus marinus (Levine), the causative agent of Dermo disease, were similar. However, mortality trends were markedly different at each site; the CB strain being notable for accelerated mortality following infection with P. marinus. In addition, hybrids between CB and all four of the regional strains exhibited similar accelerated mortality in response to infection. Mortality was strongly correlated with infection only at the high salinity site implicating interaction of differences in both oyster strain and virulence of Dermo between moderate and high salinity areas as factors in differential mortality across sites.     

Effect of low salinity on the expression profile of Na+/K+‐ATPase and the growth of juvenile chub mackerel (Scomber japonicus Houttuyn)

Chub mackerel (Scomber japonicus Houttuyn) is one of the most commercially important scombroid fish used as a food resource. Recently, there has been a demand for efficient rearing methods of this fish for a full‐life cycle aquaculture. In the present study, we evaluated the physiological responses in the juvenile S. japonicus to different ambient salinities. A significantly higher gain of the body mass was observed in the juveniles reared in 24 g/L and 13 g/L seawater than in those reared in natural seawater (34 g/L) within 40 days of the experimental period without affecting mortality. A principal enzyme for osmoregulation, Na⁺/K⁺‐ATPase, was expressed in the ionocytes located in the gill filaments of the juveniles. The number and the cell size of ionocytes and the enzymatic activity of Na⁺/K⁺‐ATPase in the gills decreased within 10 days after the low‐salinity challenge, which implies the reduction of the energy‐consuming active ion secretion under the low‐salinity environment. The physiological capacity for adaptation to low‐salinity seawater in chub mackerel could be basic knowledge to carry out culturing of these fish in coastal sea pens where ambient salinity fluctuates. The improvement of the growth performance by rearing in low‐salinity seawater will contribute to the efficient production of the seed juveniles for aquaculture.     

Ambient salinity and osmoregulation,energy metabolism and growth in juvenile yellowtail kingfish (Seriola lalandi Valenciennes 1833) in a recirculating aquaculture system

The effects of salinity on plasma osmolality, branchial chloride cell density, feed consumption and conversion and growth performance of yellowtail kingfish (Seriola lalandi) were evaluated. Fish (11.6 ± 0.6 g) were kept for 29 days at 14, 18, 22, 26 (experimental) and 30 g L^?1 (control) salinity in independent, pilot‐scale recirculation aquaculture systems. No differences in plasma osmolality or chloride cell numbers in gills were observed, pointing to a strong osmoregulatory capacity in the juveniles. Fish at 14, 18 and 22 g L^?1 (7.61 ± 0.19, 7.61 ± 0.01 and 7.61 ± 0.13% day^?1, respectively) had higher growth rates than fish at 26 and 30 g L^?1 (7.10 ± 0.05 and 6.97 ± 0.06% day^?1 respectively). The higher growth rate at lower salinity resulted from increased feed intake; feed conversion was not different. An evaluation of the impact of salinity on growth rate of on‐growing stages (till market size) seems warranted to assess whether the profitable effects of low salinity persist in later stages of this important aquaculture species.     

Effect of recovery salinity on survival of acutely stressed halibut (Hippoglossus hippoglossus L) larvae

First‐feeding halibut larvae (245‐day degrees; 40 days post hatch), reared at 34 g L^?1 salinity and 7°C, were subjected to handling and allowed to recover in a range of salinities (0–34 g L^?1) and at 10°C. Survival of the unfed larvae was determined daily for 18 days. Mortality rates approached 0 after 4 days in all treatments and presumed starvation‐induced mortality started at about 11 days post handling. By 20 days post treatments, all larvae had died. Salinities in the range of 10–20 g L^?1 produced significantly (anova , P<0.01) higher initial survival (71–95%) than salinities above 20 g L^?1 (24–48%) or below 10 g L^?1 (0–19%) and this survival pattern changed little in unfed larvae for the first 10 days following the stressor. For example, 24 hour post handling, survival of halibut was improved from 28.7±16.5% (mean±standard error, n=3) at 34.0 g L^?1 to 95.2±4.8% at 13 g L^?1. A second‐order polynomial regression of 4‐day post‐handling survival data (y=?0.002x ²+0.0603x+0.0699, r²=0.3936) predicted a maximum survival at 15.1 g L^?1 salinity. These results have important implications for halibut aquaculture and research when handling of larvae is unavoidable. For practical applications, we recommend reducing salinity of receiving waters to 15–20 g L^?1 with a slow (3–4 days) reacclimation to ambient conditions.     

Effects of frequency and amplitude of salinity fluctuation on the growth and energy budget of juvenile Litopenaeus vannamei (Boone)

The effects of salinity fluctuation on the growth, intermoult period and energy budget of juvenile Litopenaeus vannamei were investigated. Salinity fluctuation regimes were set in different frequencies of 2, 4 and 8 days and different amplitudes of ±2, ±5 and ±10 g L^?1 from a control salinity of 20 g L^?1. After a 48‐day feeding trial, the intermoult period of shrimp became shorter with increasing amplitude and frequency of salinity fluctuation (P<0.05). Both the frequency and the amplitude of salinity fluctuation had a significant effect on the growth rate of L. vannamei juveniles (P<0.05). At the frequency of 4 days, the highest growth rates occurred at amplitudes of 5–10 g L^?1, whereas the growth rate was the lowest at 10 g L^?1 when the frequency was reduced to 2 days. Feed intake (FI) and assimilation efficiency (AE) of shrimp were also significantly affected by the salinity fluctuation (P<0.05) and matched the growth rate response. The energy expenditures for growth (G), respiration (R), excretion (U) and exuviae (E) to the energy consumed as food (C) were not affected by salinity fluctuation. However, salinity fluctuation significantly affected the percentage of C as faeces (F), with the lowest value occurring at salinity amplitudes of 5–10 g L^?1 and frequencies of 4–8 days. Therefore, salinity fluctuations (every 4 days by ±5–10 g L^?1) result in higher growth rates than constant salinity conditions (20 g L^?1) through greater FI, enhanced feed assimilation and reduced faecal energy loss.     

Feeding,egg production and laboratory culture of Schmackeria poplesia Shen (Copepoda: Calanoida)

Copepods are candidates with great potential as live prey for rearing fish larvae and juveniles in aquaculture; however, the techniques for a large‐scale culture of copepods are yet to be developed. In this study, we examined the effects of water temperature, salinity, prey concentration and algal species on the grazing and egg production rates of a calanoid copepod Schmackeria poplesia (Copepoda: Calanoida). The results showed that the grazing rate of S. poplesia was the highest when the copepods were cultured in seawater with temperature of 25 °C, salinity of 20 g L^?1, prey concentration at 10⁵ cells mL^?1 and supplied with Platymonas helgolandica as the prey. The egg production rates, however, was the highest when copepods were fed with a mixed prey of Isochrysis galbana and Phaeodactylum tricornutum (cell ratio 1:1, prey concentration 10⁵ cells mL^?1) at 25 °C, 20 g L^?1 of salinity. A 100 L cultural system was established to culture S. poplesia under the condition optimized for egg production. The total number of copepods increased 40–43‐fold with the production rates of 87–290 copepods L^?1 day^?1 in 14 days. This research was the first attempt for a large‐scale culture of S. poplesia and the technique established can be further applied in aquaculture.     

Effects of changes in environmental factors on the non-specific immune response of Nile tilapia, Oreochromis niloticus L.

Lysozyme acts as a non‐specific defence substance and is found in the peripheral blood, cutaneous mucus and certain tissues of marine and freshwater fishes. In the present study, we examined the effect of various environmental factors (water temperature, salinity, pH and suspended sediments) on plasma lysozyme activity in the Nile tilapia, Oreochromis niloticus L. When the fish were reared at different water temperatures (18.4, 23, 28 and 33°C), plasma lysozyme activity increased at 28°C after 2 and 4 weeks. A significant decrease in lysozyme activity was found in the fish reared at 33°C for 4 weeks. These results suggest that there is a water temperature range that affects the amount of plasma lysozyme activity that can be detected. Fish cultured at 24 g L^?1 of salinity for 2 and 4 weeks and 12 g L^?1 for 4 weeks resulted in significantly increased plasma lysozyme activity, suggesting that environmental salinity also affects the amount of plasma lysozyme that can be detected. Lysozyme activity also significantly increased when the fish were held in acidic water at pH 4.0 and in suspended sediments at 2000 mg L^?1 for 2 weeks. It was concluded that changes in some aquatic environmental factors affect the non‐specific immune responses of Nile tilapia.     

Ionic manipulation of inland saline groundwater for enhancing survival and growth of Penaeus monodon (Fabricius)

A series of four trials were conducted on inland saline groundwater of 58 g L^?1 diluted to lower salinities up to 10 g L^?1 and later manipulating its ionic concentrations to enhance the survival and growth of Penaeus monodon postlarvae (PL). In the first experiment, the survival of PL was tested at several salinities (10, 20, 30, 40, 50 and 58 g L^?1), and the survival of PL was studied in comparison with natural sea water of similar salinities. Complete mortality of PL was observed at all salinity levels within 144 h. Longest survival for 96 h followed by 72 h was found at 10 and 20 g L^?1 salinity respectively. In the second experiment, survival of PL was tested at 10–20 g L^?1 salinity at different concentrations of calcium varying between 100 and 300 mg L^?1. The survival of PL could be increased to 7 days at 12.5 g L^?1 salinity by reducing the calcium level to 200 from 921.8 mg L^?1 with magnesium and potassium levels of 208.5 and 30.03 mg L^?1 respectively. In the third experiment, the survival of PL could be further enhanced to 18 days at the same salinity by increasing the magnesium level from 208.5 to 400 mg L^?1 with potassium held at 30.03 mg L^?1. Survival and growth of PL in inland saline water of 12.5 g L^?1 salinity similar to performance in sea water of the same salinity was achieved by increasing the potassium concentration from 30.03 to 200 mg L^?1 with calcium and magnesium levels of 199.5 and 199.4 mg L^?1 respectively.     

Effects of salinity and temperature on the growth and survival of New Zealand shortfin,Anguilla australis,and longfin,A. dieffenbachii,glass eels

The ideal water conditions for maximizing the performance of the nursery culture of glass eels harvested from the wild for aquaculture need to be determined for the New Zealand shortfin (Anguilla australis) and longfin (Anguilla dieffenbachii) eels. This study determined the survival and growth of glass eels reared under different temperature and salinity conditions in the laboratory. The growth and survival of shortfin and longfin glass eels reared in salt water (35‰) maintained at 25 °C was examined over 84 days from capture. The mean specific growth rate (SGR) was higher in shortfin [2.30±0.29% body weight (b.w.) day^?1] than longfin glass eels (1.52±0.06% b.w. day^?1), and survival was also higher in shortfin (76.0±4.16%) than for longfin glass eels (28.7±6.36%). A second experiment identified the effect of salinity (0, 17.5‰ and 35‰) and temperature (17.5 and 26.5 °C) on the acclimation, growth performance and survival of shortfin and longfin glass eels over a period of 84 days from capture. There was no incidence of mortality for either shortfin or longfin glass eels reared across all salinity treatments (0‰, 17.5‰ and 35‰) at 26.5 °C, while survival of shortfin and longfin glass eels reared at 17.5 °C was the highest in 17.5‰, followed by 35‰ and 0‰ treatments. Both temperature and salinity affected the SGR of shortfin glass eels, with the highest SGR observed for shortfin glass eels reared in 0‰ water maintained at 26.5 °C. In longfin glass eels, salinity alone had an effect on the SGR, with the highest SGR observed in glass eels reared in 0‰ water regardless of the water temperature (17.5 and 26.5 °C). In addition, the adaptability of glass eels to salinity was evaluated from the development and the physiological responses of gill chloride cell (CC) morphology. The number and size of CCs increased significantly with increasing salinity in both shortfin and longfin eels.     

Combined effects of salinity and potassium concentration on juvenile mulloway (Argyrosomus japonicus, Temminck and Schlegel) in inland saline groundwater

This paper reports on experiments conducted to examine the combined effects of salinity and potassium concentration on survival and growth of juvenile mulloway (Argyrosomus japonicus, Temminck and Schlegel) in inland saline groundwater. Three separate experiments were conducted in 20 (±1)°C water. In the first experiment, mulloway were held in 60 L aquaria (triplicate) with salinities of 5, 15, 25 or 35 g L^?1 and potassium concentrations of 20%, 40%, 60% or 80% of the concentration present in oceanic water of the equivalent salinity in a 4 × 4 factorial combination for 7 days. Response surface contour diagrams were generated from survival data to estimate optimal conditions. The results showed that maximum survival of juvenile mulloway occurred at salinities of >14 g L^?1 and potassium concentrations of >38%. Survival was lowest at salinities of <7 and >33 g L^?1 and potassium concentrations of <25%. The second experiment was conducted with mulloway held in 60 L aquaria at salinities of 15, 25 or 35 g L^?1 and potassium concentrations of 40%, 60%, 80% or 100% in a 3 × 4 factorial combination for 44 days. Optimal conditions for maximum survival and growth of mulloway were within a salinity range of 15–35 g L^?1 and potassium concentration above 40%. The third experiment was conducted in three 500 L tanks to record the survival and growth of mulloway fingerlings held at 20 (±1)°C, 23 g L^?1 salinity and potassium concentrations of 50% for 8 months. Survival and growth of mulloway fingerling in inland saline groundwater were similar to those reported from a semi‐intensive floating tank system in inland saline water and sea cage trials in oceanic water.     

Growth, feed utilization and growth heterogeneity in juvenile turbot Scophthalmus maximus (Rafinesque) under different photoperiod regimes

Juvenile turbot (45 g, SE = 1.3) were reared under three photoperiods, 08L:16D, 12L:12D and 20L:04D at slightly elevated ambient temperature for Ireland. Over the 297‐day experimental period, the overall growth rate of the 12L:12D (0.82% d^?1) treatment was higher than for both 08L:16D (0.80% d^?1) and 20L:04D (0.77% d^?1). Overall relative feed intake (FI = % consumption*day^?1) was higher for the 20L:04D (FI = 0.81% d^?1, SE = 0.06) treatment than for the 08L:16D (0.63% d^?1, 0.04) and 12L:12D (0.64% d^?1 0.04) treatments, whereas feed conversion efficiency (FCE = weight gain* consumption^?1) was lower in the 20L:04D (FCE = 0.67, SE = 0.08) group when compared with the 08L:16D (0.88, 0.06) and 12L:12D (0.88, 0.06) treatments. Present results show that the long‐term extended fixed photoperiod may act as an irritant, inducing stress, suppressing growth and reducing feed utilization. It is hypothesized that the progression of size‐dependent hierarchies over time can be divided into two distinct phases herein referred to as ‘hierarchy resolution’ and ‘hierarchy stabilization’ phases (or phases 1 and 2) characterized by increasing and decreasing growth heterogeneity respectively. Growth heterogeneity is measured as coefficient of variation of weight and rank correlation of initial weight of a phase and corresponding growth rate.     

Incubation of European Squid (Loligo vulgaris Lamarck, 1798) eggs at different salinities

Loligo vulgaris is a commercially important squid throughout the Mediterranean region and is a candidate species in biomedical and aquaculture research. Some loligo species (L. opalescens, L. forbesi, Sepiteuthis lessoniana) have now been cultured through some successive generations in closed, recirculating seawater systems. The effects of salinity on hatching European Squid (L. vulgaris Lamarck, 1798) eggs were investigated during November 2004. The egg capsules were incubated directly in salinity of 32, 34, 36, 38, 40, 42 and 37 g L^?1 (control group) at 19.8°C (SD 1.2°C), and a photoperiodicity of 12 h light:12 h dark for 16–23 days before hatching. In all treatments, the eggs were developed and hatched normally after 16–22 days at 32 g L^?1, 17–22 days at 34, 18–21 days at 42 g L^?1, 18–22 days at 36 and 40 g L^?1, 19–22 days at 37 g L^?1 and 19–23 h at 38 g L^?1. In the experiments, the highest hatching rate and hatching success (HS) of the eggs were obtained at 38 g L^?1 (hatching rate: 100% (SD 0%) and HS: 96.7% (SD 3.5%)) and the lowest hatching rate at 42 g L^?1 (hatching rate: 3% (SD 6%) and HS: 0%). Dorsal mantle lengths (DML) of new hatchlings ranged from 2.08 to 2.80 mm. The present study showed that salinity affects the hatching rate and HS of eggs and first hatching time and DML of paralarvae in L. vulgaris. The squid eggs at stage 11 (I) can tolerate 5 g L^?1 reduction and 3 g L^?1 increase in salinity.     

Effects of salinity on osmoregulation,growth and survival in Asian swamp eel (Monopterus albus) (Zuiew 1793)

The Asian swamp eel Monopterus albus is normally considered a freshwater species, but can also occasionally be found in brackish water. It is an obligate air‐breather with highly reduced gills, making its osmoregulation physiology interesting because the gills normally represent the primary site of osmoregulation in teleosts. Being a popular fish for human consumption, the swamp eel is cultured extensively in freshwater ponds in the Mekong Delta of Vietnam. However, very little is known about its salinity tolerance, which is becoming topical due to the increasing salt‐water intrusions into tropical deltas. We therefore studied how increased salinity affects survival, growth, blood pressure, heart rate, blood osmolality and plasma ions. All eels survived prolonged exposure to 5 and 10 g L^?1, although plasma osmolality increased significantly at 10 g L^?1. Further elevation to 15 and 20 g L^?1 was associated with significantly elevated mortality, with a corresponding increase in plasma osmolality and ion con‐centrations. Our results show that swamp eels thrive in 0–10 g L^?1 with an optimum growth between 0 and 9 g L^?1, indicating that utilization of low saline brackish waters for aquaculture is possible.     

Effect of salinity on carrying capacity of adult Nile tilapia Oreochromis niloticus L. in recirculating systems

Effect of salinity on carrying capacity of a recirculation system for Nile tilapia, Oreochromis niloticus L.; production was assessed. Survival, growth and feed conversion ratio of adult Nile tilapia fed 30% crude protein diet for 88 days were measured at three different salinity levels (8, 15 and 25 g L^?1) and two stocking densities (20 and 40 m^?3) in three independent recirculating systems. Highest survival (98%) and a linear growth in net biomass (P<0.01) was observed in both densities at 8 g L^?1 and in 20 m^?3 treatment at 15 g L^?1. Highest net biomass growth was observed in the 40 m^?3 stocking density treatment at 8 g L^?1 salinity level (P<0.05). Overall biomass growth was significantly affected by salinity indicating a decrease in Nile tilapia carrying capacity with increased salinity. About 11 000 kg ha^?1 crop^?1 of Nile tilapia can be obtained in recirculating systems at 8 g L^?1 salinity, significantly higher than the net production at 15 g L^?1 (5200 kg ha^?1 crop^?1) and 22 g L^?1 (4425 kg ha^?1 crop^?1).     

Acute toxicity of nitrite on white shrimp Litopenaeus vannamei (Boone) juveniles in low‐salinity water

The nitrite toxicity was estimated in juveniles of L. vannamei. The 24, 48, 72 and 96 h LC₅₀ of nitrite‐N on juveniles were 8.1, 7.9, 6.8 and 5.7 mg L^?1 at 0.6 g L^?1; 14.4, 9.6 8.3 and 7.0 mg L^?1 at 1.0 g L^?1; 19.4, 15.4, 13.4 and 12.4 mg L^?1 at 2.0 g L^?1 of salinity respectively. The tolerance of juveniles to nitrite decreased at 96 h of exposure by 18.6% and 54.0%, when salinity declined from 1.0 to 0.6 g L^?1 and from 2.0 to 0.6 g L^?1 respectively. The safe concentrations at salinities of 0.6, 1.0 and 2.0 g L^?1 were 0.28, 0.35 and 0.62 mg L^?1 nitrite‐N respectively. The relationship between LC₅₀ (mg L^?1), salinity (S) (g L^?1) and exposure time (T) (h) was LC₅₀ = 8.4688 + 5.6764S – 0.0762T for salinities from 0.6 to 2.0 g L^?1 and for exposure times from 24 to 96 h; the relationship between survival (%) and nitrite‐N concentration (C) for salinity of 0.6–2.0 g L^?1, nitrite‐N concentrations of 0–40 mg L^?1 and exposure times from 0 to 96 h was as follows: survival (%) = 0.8442 + 0.1909S – 0.0038T – 0.0277C + 0.0008ST + 0.0001CT–0.0029SC, and the tentative equation for predicting the 96‐h LC₅₀ to salinities from 0.6 to 35 g L^?1 in L. vannamei juveniles (3.9–4.4 g) was 96‐h LC₅₀ = 0.2127 S² + 1.558S + 5.9868. For nitrite toxicity, it is shown that a small change in salinity of waters from 2.0 to 0.6 g L^?1 is more critical for L. vannamei than when wider differences in salinity occur in brackish and marine waters (15–35 g L^?1).     

Effects of hypoxia and hyperoxia on growth and food conversion efficiency in the spotted wolffish Anarhichas minor (Olafsen)

Abstract The effect of water oxygen content on growth and food conversion efficiency was evaluated for juvenile spotted wolffish, mean (± SD) initial weight 68.5 (± 17.5) g, reared at oxygen levels of 4.0, 6.0 (hypoxia), 9.6 (normoxia) and 14.5 (hyperoxia) mg L^?1 for 11 weeks at 8 °C. Mean weights and total food consumption were significantly higher in the control and hyperoxic groups compared with the hypoxic groups at the end of the experiment. The 9.6 and 14.5 mg L^?1 groups exhibited significantly higher overall specific growth rates (0.90 and 0.86% day^?1 respectively) compared with the groups on 4.0 and 6.0 mg L^?1 (0.46 and 0.71% day^?1 respectively). In the hyperoxic group, growth was only limited in the first period and, in the hypoxic groups, growth rates increased throughout the experiment, with the 6.0 mg L^?1 group performing equally well compared with the control in the last period. Overall, our findings suggest that the species will adapt to both high and low ambient water oxygen content given a period of adaptation. After the adaptation phase, growth and food conversion efficiency are comparable in the oxygen level range of 6.0–14.5 mg L^?1.     

In situ hypochlorous acid generation for the treatment of brackish shrimp aquaculture wastewater

This study presents an unconventional framework for treating shrimp aquaculture wastewater based on in situ hypochlorous acid (HOCl) oxidation. The in situ oxidation process makes use of the salinity present in aquaculture wastewater to generate HOCl. The undivided electrolytic cell consisted of two sets of graphite as the anode and stainless sheets as the cathode. The electrochemical oxidation of shrimp aquaculture wastewater was carried out for an influent COD concentration of 1730 mg L^?1 at current densities of 37.2 and 74.5 mA cm^?2. The results showed that in order to achieve a residual COD concentration of 50±5 mg L^?1 at current densities of 37.2 and 74.5 mA cm^?2, electrolysis periods of 60 and 30 min are required respectively. Hence, for the above‐mentioned current densities, the corresponding energy requirements were found to be 19.4 and 13.3 W h L^?1. The cost incurred in treating 1 m³ of shrimp aquaculture wastewater was found to be RM 4 and 3 when the electrolytic reactor was operated at a current density of 37.2 and 74.5 mA cm^?2 with a salinity of 23‰. The foregoing study highlights the potential of in situ HOCl oxidation in treating brackish shrimp aquaculture wastewater.