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.     

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.     

Isolation and culture of the marine rotifer, Colurella dicentra (Gosse, 1887), from a Mississippi Gulf Coast estuary

Few marine rotifer species (e.g. Encentrum linheii and Synchaeta cecilia) have been cultured successfully besides Brachionus plicatilis and B. rotundiformis, commonly used to rear larvae of many marine fish species. The development of culture techniques for marine rotifers smaller in size than the Brachionus species may be useful for rearing fish species for which the currently used prey are too large. We evaluated the possibility of culturing Colurella dicentra isolated from a Mississippi Gulf Coast estuary. An experiment was conducted to determine the effects of salinity (10–35 g L^?1) on its population growth rate. Rotifers were fed Nannochloropsis oculata at a density of 100 000 cells mL^?1 for 15 days. Colurella dicentra survived in water with a salinity of 10–47 g L^?1. Densities of up to 300 rotifers mL^?1 were sometimes attained in cultures. Salinity influenced C. dicentra production (P<0.001). The mean rotifer numbers at 10 g L^?1 (22 840±2604 SD), 15 g L^?1 (25 980±7071 SD) and 20 g L^?1 (19 780±1029 SD) at the end of the experiment were similar (P>0.05), but were higher (P=0.05) than numbers at 25 g L^?1 (4240±1783), 30 g L^?1 (1300±264 SD) and 35 g L^?1 (100±101 SD). The population growth rate (r) of the rotifers was the highest at 15 g L^?1 (0.37–0.42 day^?1), and the lowest at 35 g L^?1 (?0.33–0.06 day^?1). This is the first report of C. dicentra in the estuarine waters of the Gulf of Mexico, and also the first time it has been cultured successfully.     

Influence of salinity, diurnal rhythm and daylength on feeding in Laternula marilina Reeve

A nature‐simulating culture system was used to explore the influence of salinity, the diurnal cycle and daylength on ingestion rate (IR) and assimilation efficiency (AE) of Laternula marilina. The clams used in the experiments were grouped into three sizes: large, medium and small according to shell length and dry fresh weight. The clams in all size groups demonstrated a common response pattern in IR and AE under salinities ranging from 18 to 34 g L^?1. The clams achieved the greatest IR within the salinity range 27–30 g L^?1. There was a marked reduction in IR outside this range. Of the salinities tested 18 g L^?1 was the harshest stress to the feeding of L. marilina. Between the salinities of 24 and 34 g L^?1, the AE of the clam responded in an inverse way to that of IR, suggesting that L. marilina is able to compensate for the loss of IR by an increase in AE. Although the differences between clam size groups were not statistically different, those between different salinities were except those between 27 and 34 g L^?1 (IR) and 23 and 34 g L^?1 (AE). All sizes of clam showed a two‐phase diurnal feeding pattern, a high ingestion phase from 00:00 to 08:00 hours and a low ingestion phase from 12:00 to 20:00 hours. The response of feeding (as measured by IR) to daylength comprised high and constant feeding at daylengths from 0 to 16 h and declining and unstable feeding as daylength increased from 16 to 24 h. All sizes of clams demonstrated an inverse adaptation to AE compared with IR, indicating that the clam is able to achieve a stable feeding physiology by compensating for daylength‐induced variations in IR by changing AE.     

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.     

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).     

Genetic effects influencing salinity tolerance in six varieties of tilapia (Oreochromis) and their reciprocal crosses

Six tilapia varieties were used in two 6 × 6 diallel crosses. Salinity was increased in daily increments of 7 g L^?1 in five replicate trials to estimate the salinity tolerances of 2205 F₁ juveniles from parental varieties and their reciprocal crosses. Genetic effects potentially influencing salinity tolerance were estimated, including line effects, maternal effects, reciprocal and specific reciprocal effects, direct heterosis, specific combining abilities (SCAs) and general combining abilities (GCAs). The mean heterosis, , for salinity tolerance was 4.46 g L^?1 (P<0.01). The average mean salinity tolerance (MST) of the parental varieties was 35.2 g L^?1, and yet, MSTs above 36 g L^?1 were found in 21 of 34 variety crosses produced. In some instances, maternal effects offset line effects, while in others, these influences were complementary. Ten variety combinations exhibited significant (P<0.05) or highly significant (P<0.01) direct heterosis, and SCAs were significant (P<0.05) or highly significant (P<0.01) in five combinations. Reciprocal and specific reciprocal effects also influenced the salinity tolerance in some variety combinations. Direct line effects generally reflected MST rankings. The variance of cross means was 30.1% due to variety GCAs (primarily additive effects) and 69.9% due to SCAs (primarily dominance effects).     

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.     

Novel effects of salinity and water reuse on growth of juvenile New Zealand turbot, Colistium nudipinnis (Waite 1910), a potential aquaculture species

Juvenile New Zealand turbot, Colistium nudipinnis (Waite 1910), produced during the first aquaculture development project for this endemic flatfish, were reared at ambient and reduced salinities to determine the effect of salinity on growth and survival and the possible implications for aquaculture. Juveniles aged from 176 days to 17 months showed a high level of salinity tolerance, with minimal mortality attributable to salinity reduction over the range 33–18 g L^?1. Growth rate was slightly increased at the slightly reduced salinity of 28 g L^?1 (5 g L^?1 below ambient) but was significantly decreased at the markedly reduced salinity of 18 g L^?1. The growth response at 23 g L^?1 was markedly different between ‘new’ water and water that was recycled from a previous set of rearing tanks, with juveniles reared in 23 g L^?1‘new’ having a mean growth rate that was 29% lower than that of the control juveniles (in 33 g L^?1‘new’ water), whereas juveniles in 23 g L^?1‘reused’ water grew 45% faster than the controls. The implications of this novel effect are discussed in relation to the aquaculture potential of the New Zealand turbot.     

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.     

Short-term responses of adult kuruma shrimp Marsupenaeus japonicus (Bate) to environmental salinity: osmotic regulation, oxygen consumption and ammonia excretion

The effects of salinity on haemolymph osmolality, oxygen consumption and ammonia excretion were investigated in adult kuruma shrimp, Marsupenaeus japonicus (Bate), at salinities of 20, 25, 30 and 35 g L^?1. Haemolymph osmolality showed a positive linear relationship (r²=0.9854) with medium osmolality. The isosmotic point calculated from this relationship was 1039 mOsm kg^?1, which corresponds to a salinity of approximately 35 g L^?1. The slope of the regression equation was very high (0.81), suggesting that M. japonicus adults are poor osmoregulators compared with the adults of other penaeids and to conspecific young. The difference between haemolymph and medium osmolality (D_OP) was lowest at 35 g L^?1 and highest at 20 g L^?1. Thus, the minimum D_OP coincided with the isosmotic point of the shrimp. The respiration rate was significantly lower at 30 g L^?1 than at the other salinities. Ammonia excretion rates were inversely related with salinity and therefore were minimal at 35 g L^?1. The results of this study suggest that the optimum salinity for adult kuruma shrimp is around 30–35 g L^?1 and that even minor (e.g. 5 g L^?1) deviations from this optimum cause significant physiological changes. Further, the observed increases in oxygen consumption and ammonia excretion during exposure to low salinities, which indicate higher energy expenditure and amino acid catabolism for osmoregulation, respectively, suggest that the growth efficiency of M. japonicus adults may be severely compromised by hypohaline water inflow into the rearing ponds.     

Effects of temperature and salinity on the survival and development of mud crab, Scylla serrata (Forsskål), larvae

The combined effects of temperature and salinity on larval survival and development of the mud crab, Scylla serrata, were investigated in the laboratory. Newly hatched larvae were reared under 20 °C temperature and salinity combinations (i.e. combinations of four temperatures 25, 28, 31, 34 °C with five salinities 15, 20, 25, 30, 35 g L⁻¹). The results showed that temperature and salinity as well as the interaction of the two parameters significantly affected the survival of zoeal larvae. Salinity at 15 g L⁻¹ resulted in no larval survival to the first crab stage, suggesting that the lower salinity tolerance limit for mud crab larvae lies somewhere between salinity 15 and 20 g L⁻¹. However, within the salinity range of 20–35 g L⁻¹, no significant effects on survival of zoeal larvae were detected (P>0.05). The combined effects of temperature and salinity on larval survival were also evident as at low salinities, both high and low temperature led to mass mortality of newly hatched larvae (e.g. 34 °C/15 g L⁻¹, 34 °C/20 g L⁻¹ and 25 °C/15 g L⁻¹ combinations). In contrast, the low temperature and high salinity combination of 25 °C/35 g L⁻¹ resulted in one of the highest survival to the megalopal stage. It was also shown that at optimal 28 °C, larvae could withstand broader salinity conditions. Temperature, salinity and their interaction also significantly affected larval development. At 34 °C, the mean larval development time to megalopa under different salinity conditions ranged from 13.5 to 18.5 days. It increased to between 20.6 and 22.6 days at 25 °C. The effects of salinity on larval development were demonstrated by the fact that for all the temperatures tested, the fastest mean development to megalopa was always recorded at the salinity of 25 g L⁻¹. However, a different trend of salinity effects was shown for megalopae as their duration consistently increased with an increase in salinity from 20 to 35 g L⁻¹. In summary, S. serrata larvae tolerate a broad range of salinity and temperature conditions. Rearing temperature 25–30 °C and salinity 20–35 g L⁻¹ generally result in reasonable survival. However, from an aquaculture point of view, a higher temperature range of 28–30 °C and a salinity range of 20–30 g L⁻¹ are recommended as it shortens the culture cycle.     

Effects of salinity and temperature during incubation on hatching and development of lingcod Ophiodon elongatus Girard, embryos

The interactive effects of salinity and temperature on development and hatching success of lingcod, Ophiodon elongatus Girard, were studied by incubating eggs at four temperatures (6, 9, 12 and 15°C) and five salinities (15, 20, 25, 30 and 35 g L^?1). Hatch did not occur in any of the 15°C treatments. Degree days (°C days) to first hatch was not influenced by temperature or salinity, however, calendar days to first hatch differed significantly for temperature (P<0.0001, 61±1, 44±1 and 35±1 days for 6, 9 and 12°C respectively). Degree days to 50% (427.1±4.2) hatch was not significantly influenced by temperature but was by salinity (P=0.0324). Viable hatch (live with no deformities, 74.1±4.0%) was greatest at 9°C and 25 g L^?1 but not significantly different in the range of 20–30 g L^?1. Larval length (9.4±0.13 mm) was greatest at 9°C and 20–30 g L^?1. Temperature and salinity significantly influenced all categories of deformities with treatments at the upper (12°C and 35 g L^?1) and lower limits (6°C and 15 g L^?1) producing the greatest deformities. The optimal temperature and salinity for incubating Puget Sound lingcod eggs was found to be 9°C and 20–30 g L^?1.     

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.     

Effect of salinity on reproductive performance of Acanthopagrus latus (Houttuyn) in spawning tanks

More than 250 male and female yellowfin seabream (Acanthopagrus latus) were caught in the creeks near the Mahshar area in the north‐west of Persian Gulf using fishhooks to study the effects of salinity on reproductive indices. The experiments were carried out using three salinity treatments (30 ± 1 g L^?1, 35 ± 1 g L^?1 and 40 ± 1 g L^?1) with three replications. A total of six males and three females were randomly introduced to each tank. The survival rate of the broodstock was estimated at more than 90% at different salinity levels and the maximum rate was observed at 30 g L^?1 of the experiment rate. The percentage of buoyant eggs was more than 90% at 40 g L^?1 and it was significantly different from other treatments. The average number of eggs per female (312 914 ± 65 085), and the average number of eggs per kilogram of female (649 460 ± 173 574) at 40 g L^?1 were more than those in the other treatments but no significant differences were observed (P ≤ 0.05). The average percentage of fertilized eggs (86.7%) and the average percentage of hatched larvae (67%) at 40 g L^?1 treatment was more than those at 30 g L^?1 and 35 g L^?1 treatments but no significant differences were observed (P ≤ 0.05). At 40 g L^?1 salinity, in all spawning cases, the released eggs were hatched. Overall, the present study has shown that better buoyant eggs of A. latus can be obtained at salinity 40 g L^?1. On the other hand, the percentage of fertilized eggs and hatched larvae were not affected by salinity.     

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.     

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.     

Are egg production and respiration of the marine pelagic copepod Acartia steueri influenced by crowding?

The understanding of the biological responses of copepods under crowding conditions contributes to establish their stable cultures at high densities for aquaculture industry, which are preferred live feeds for fish larvae. The present study investigated survivorship, fecundity, hatching success and respiration rate, of Acartia steueri raised under five densities, from 100 to 2,000 ind. L^?1, to clarify the biological responses of the copepod under dense culture. There were no significant differences in survival, fecundity and hatching success among all density conditions, whereas the respiration rate at 2,000 ind. L^?1 decreased by 80% as compared with a condition at 100 ind. L^?1. The female copepods raised under a copepod density of >500 ind. L^?1 probably invested a larger proportion of energy in reproduction in relation to total assimilated energy as compared with females under lower copepod densities. This change of energy allocation may allow A. steueri under high densities to maintain high fecundity. Acartia steueri might be a promising species for dense culture because its mortality and fecundity were independent of the effect of crowding, and the density‐dependent reduction in the metabolic rate might increase reproductive investment to maintain a constant rate of reproduction even under high densities.     

Use of the microalga Nannochloropsis occulata in the rearing of newborn longsnout seahorse Hippocampus reidi (Syngnathidae) juveniles

The aim of this study was to evaluate the effect of microalgae on the rearing of newborn juveniles of the longsnout seahorse, Hippocampus reidi. Two treatments in three replicates were tested over a 15‐day period: with and without the addition of the microalgae Nannochloropsis oculata at a concentration of 2.02 ± 0.44 × 10⁶ cells mL^?1. At each replicate, beginning on the second day of life, 120 H. reidi juveniles (stocking density of 3 ind L^?1) were fed the offspring of the benthic copepod Tisbe biminiensis (100 copepod cm^?2) together with newly hatched Artemia nauplii (3.8 mL^?1). From the sixth day of life, enriched Artemia metanauplii replaced newly hatched Artemia nauplii. After 15 days, the H. reidi individuals were counted, measured and weighed. Mean survival was significantly greater in the microalgae treatment (76.42 ± 5.07%) than in the treatment with no microalgae (25.44 ± 6.91%). Moreover, total length, height and dry weight were significantly larger in the microalgae treatment. Thus, the addition of microalgae increases the growth and survival of H. reidi juveniles fed T. biminiensis and Artemia. The higher growth and survival of H. reidi juveniles was not related to the larger ingestion rates but probably to the nutritional improvement of the live feeds or to the probiotic effect. The protocol developed for rearing H. reidi juveniles resulted in a high survival, and represents an advance in the farming of this species.