Effects of temperature on survival and growth of juvenile spinefoot rabbitfish (Siganus rivulatus)

Interest in culturing marbled spinefoot rabbitfish Siganus rivulatus is increasing in countries on the Eastern Mediterranean, Red Sea and Arabian Gulf. However, information on environmental tolerances and requirements for optimal growth are scarce. In the present work, the temperature requirements for spinefoot rabbitfish were investigated in two experiments. In the first experiment, juvenile rabbitfish were distributed into eight 180 L square tanks at 12 fish per tank. The temperature in four tanks was reduced at a rate of 1 °C day^?1 and in four tanks was increased by 1 °C day^?1 until the fish stopped feeding. Minimum and maximum temperatures for feeding were recorded. In the second experiment, the fish were placed in four temperature treatments (17, 22, 27, 32 °C) at four replicates per treatment for 8 weeks. Survival and growth were evaluated. Fish stopped feeding at 14 and 36 °C. Their maximum growth rate was at 27 °C, and survival was 100% in all treatments. The relationship between specific growth rate and temperature was parabolic, described by the equation: SGR=?0.0014 (T³)+0.0798 (T²)?1.3089 (T)+6.7342. The results show that S. rivulatus is a eurythermal fish whose optimal temperature for growth is circa 27 °C.     

Growth and survival of first-feeding spotted wolffish (Anarhichas minor Olafsen) at various temperature regimes

In order to define temperature regimes that could benefit successful production of spotted wolffish (Anarhichas minor) juveniles, experiments with offspring from two different females were carried out. The larvae were fed a new formulated feed or a commercial start‐feed for marine fish, both of which have given high survival rates. In the first experiment newly hatched larvae were fed at constant 6 °C, 8 °C, 10 °C and 12 °C as well as at ambient seawater temperature (2.9–4.5 °C) during 63 days. High survival, 90% to 96%, was registered at ambient and most constant temperature regimes, whereas in the 12 °C groups survival was reduced to 80%. Growth rate (SGR) was very low, 1.8% day^?1, at the low ambient temperatures. Growth rate was positively correlated with temperature and varied between 3.1% day^?1 to 4.7% day^?1, from 6 °C to 12 °C. In the second experiment, set up to include potential detrimental temperatures and study beneficial effects of a more restricted, elevated first‐feeding temperature regime, the larvae were fed at constant 8 °C, 10 °C, 12 °C, 14 °C and 16 °C until 30 days post hatch, followed by constant 8 °C for the next 33 days. In this experiment, low survival, 25% and 2.0%, was registered at 63 days post hatch when larvae were reared initially at 14 °C and 16 °C respectively. The survival of the larvae at the other temperature regimes varied from 47% to 64%, highest survival rate (64%) was found at 8 °C. The lowest specific growth rate, 2.6% day^?1, was noted in the 16 °C group. At constant 8 °C to 14 °C (regulated to 8 °C), the SGR varied from 4.45% day^?1 to 5.13% day^?1. The larvae grew faster in the experiment when initially comparable temperatures (8 °C, 10 °C and 12 °C) were regulated to constant 8 °C after 30 days compared with the first experiment where feeding was carried out at the same constant temperatures (8 °C, 10 °C and 12 °C) during the whole experimental period.     

Effects of temperature on growth of juvenile blackfoot abalone, Haliotis iris Gmelin

The effects of temperature on growth and survival of juvenile blackfoot abalone, Haliotis iris, were investigated. Animals of 10, 30 or 60 mm initial shell length were exposed to ambient (6–10°C), 14, 18, 22 and 26°C for 112 days in a flow‐through culture system. Maximum growth occurred at 22°C for the 10 and 30 mm size classes and at 18°C for the 60 mm size class. Regression analysis identified the optimal temperature for growth (T_optG) at around 21°C for the 10 and 30 mm size classes and at 17–18°C for the largest size class. In a second experiment, the critical thermal maximum of H. iris was determined as a measure of thermal tolerance. Abalone were subjected to increasing water temperatures at a rate of 2°C h^?1 until they detached from the substrate. Abalone of 10 mm displayed greater thermal tolerance than abalone of 30 and 60 mm in length. CT₅₀ temperatures were 28.8, 27.7 and 27.8°C, yielding deduced T_optG values of 19.7, 18.3 and 18.4°C for the 10, 30 and 60 mm size classes respectively. The size‐dependent nature of the relationship between growth and temperature could be capitalized upon in recirculating aquaculture systems.     

Effects of temperature and dietary protein on the growth performance and IGF‐I mRNA expression of juvenile mirror carp (Cyprinus carpio)

Juvenile mirror carp were fed with five different diets containing 303, 322, 341, 361 and 379 g kg^?1 protein and reared at three different water temperatures (18, 23 and 28 °C) for 60 days. We investigated the insulin‐like growth factor I (IGF‐I) mRNA expression, growth performance and the relationship between IGF‐I mRNA expression and the growth performance. The results indicated that the IGF‐I mRNA expression, final body weight, specific growth rate (SGR) and feed efficiency (FE) were enhanced significantly with increasing dietary protein levels (P < 0.05), whereas the protein efficiency ratio, hepatosomatic index (HSI) and viscerosomatic index (VSI) were decreased. Moreover, the IGF‐I mRNA expression, final body weight and SGR were increased significantly with temperature, whereas the HSI and VSI indices were decreased significantly with temperature. Correlation analysis showed that the IGF‐I mRNA expression levels in the brain and liver were positively related to the SGR and FE growth indices (P < 0.01). Finally, the optimal protein requirements for fish growth in different seasons were determined based on the values of SGR and FE, that is 343–348 g kg^?1 protein at 18 °C, 354–352 g kg^?1 at 23 °C and 371–362 g kg^?1 at 28 °C. In this way, we can adjust the dietary protein levels according to culture temperature to reduce any negative impacts on dietary costs and environmental pollution.     

Effect of temperature and phytoplankton concentration of Partitioned Aquaculture System water on freshwater mussel filtration

The freshwater mussel Elliptio complanata was provided green algal‐dominated water from a Partitioned Aquaculture System (PAS) over a range of water temperatures (6.1–32.4 °C) and suspended particulate organic carbon (POC) concentrations (<1–32.2 mg C L^?1) to determine filtration rates as mg POC kg^?1 wet tissue weight h^?1. The lowest filtration rates were observed at lowest temperatures and POC concentrations while the highest rates were at intermediate temperatures and the highest POC levels. The predicted filtration rate (PFR) in response to water temperature and POC concentrations was as follows: ln PFR=1.4352+0.1192 POC+0.1399 T?0.0001 T³. Within the experimental conditions, PFRs at any POC concentration increased with increased water temperature to a peak at 22 °C and then decreased. The maximum PFR occurred at 22 °C and 32 mg C L^?1 and the minimum PFR at 7 °C and 1 mg C L^?1. A model to describe the mussel filtration rate responses to PAS water conditions involves both water temperature and POC concentration.     

Interactions between temperature and size on the growth,size heterogeneity,mortality and cannibalism in cultured larvae and juveniles of the Asian catfish,Pangasianodon hypophthalmus (Sauvage)

Temperature effects vary throughout the ontogeny, but are proportionally more variable during the early life stages than in older fish. The larvae of a few species have been studied but contrasting trajectories were observed, thereby making it difficult to predict how temperature impacts on the growth, survival and size heterogeneity in a particular species. This study examined these interactions in young [0.9 mg–1 g wet mass (WM)] Pangasianodon hypophthalmus, one of the most extensively cultured tropical fish. Fish were raised at five temperatures from 23 to 33 °C in a recirculated water system, fed in excess with a high‐energy feed (Artemia then a formulated feed, >50% protein), and examined at 1‐day (first feeding days) or 4‐day intervals (older fish). The temperature that produced the fastest growth (T°_opt) was 31 °C at the start of exogenous feeding (0.9 mg); it increased to 32.7 °C at 8 mg then decreased by 0.7 °C for each 10‐fold increase of WM. Size heterogeneity was lower and survival was higher (70–85% from 0.9 mg to 1 g) when the temperature was close to T°_opt. Comparisons with other species suggest that the slope of the relationship between T°_opt and fish size has a strong latitudinal component, and may also reflect the fish sensitivity to oxygen.     

Combined effects of photoperiod and temperature on growth and survival of African catfish (Clarias gariepinus,Burchell 1822) larvae under laboratory conditions

ABSTRACT

The effect of photoperiod (24L:00D, 12L:12D, and 00L:24D) and temperature (22 ± 1°C and 28 ± 1°C) on performance of Clarias gariepinus larvae was tested. Larvae weighing 3.2 ± 0.24 mg were cultured in aquaria at a stocking density of 20 fish L^?1 and fed twice a day on catfish starter diet (40% CP) at 10 % BW day^?1. Highest mean weight gain (31.00 mg), SGR (7.56% day^?1), and survival (83%) were achieved at photoperiod and temperature combination of 00L:24D and 28 ± 1°C. Percent survival of larvae differed significantly (p < .05) among treatments with optimal survival of (83%) in treatment combination of 28 ± 1°C and 00L:24D, while lowest survival (40%) in treatment combination of 22 ± 1°C and 24L:00D.     

Metabolic measurements and parameter estimations for bioenergetics modelling of Pacific Chub Mackerel Scomber japonicus

As a crucial step in developing a bioenergetics model for Pacific Chub Mackerel Scomber japonicus (hereafter chub mackerel), parameters related to metabolism, the largest dissipation term in bioenergetics modelling, were estimated. Swimming energetics and metabolic data for nine chub mackerel were collected at 14°C, a low temperature within the typical thermal range of this species, using variable‐speed swim‐tunnel respirometry. These new data were combined with previous speed‐dependent metabolic data at 18 and 24°C and single‐speed (1 fork length per second: FL/s) metabolic data at 15 and 20°C to estimate respiration parameters for model development. Based on the combined data, the optimal swimming speed (the swimming speed with the minimum cost of transport, U_opt) was 42.5 cm/s (1.5–3.0 FL/s or 2.1 ± 0.4 FL/s) and showed no significant dependence on temperature or fish size. The daily mass‐specific oxygen consumption rate (R, g O₂ g fish^?1 day^?1) was expressed as a function of fish mass (W), temperature (T) and swimming speed (U): R = 0.0103W^?0.490 e^(0.0457T) e^(0.0235U). Compared to other small pelagic fishes such as Pacific Herring Clupea harengus pallasii, Pacific Sardine Sardinops sagax and various anchovy species, chub mackerel respiration showed a lower dependence on fish mass, temperature and swimming speed, suggesting a greater swimming ability and lower sensitivity to environmental temperature variation.     

Nucleic acids and fatty acids of the common octopus, Octopus vulgaris, in relation to the growth rate

The aim of this study was to investigate changes in the ribonucleic acid (RNA)/deoxyribonucleic acid (DNA) ratio and the fatty acid composition of cultured Octopus vulgaris (50–750 g) in relation to recent (last 30 days) specific growth rate (SGR). Wild animals (80–500 g), collected in the field throughout the year (Aegean Sea, Mediterranean), were also examined for the aforementioned biochemical parameters. Octopuses were reared in a closed seawater system at three different temperatures (15, 20 and 25 °C). The octopuses were fed on squid (Loligo vulgaris). The cultured animals showed a high n‐3 (33–52.9%) and n‐6 (3.3–13.7%) polyunsaturated fatty acid content, but with a high variation for 22:6n‐3 [docosahexaenoic acid (DHA)], 20:5n‐3 [eicosapentaenoic acid (EPA)] and 20:4n‐6 [arachidonic acid (AA)]. The proportion of these fatty acids (% total fatty acids) and the RNA/DNA ratio were linearly (P<0.0001) related to SGR. Specifically, RNA/DNA (0.5–1.9) and AA (2.7–10.7%) increased, while EPA (10.4–19.7%) and DHA (20.8–31.9%) decreased, with increasing SGR (0.4–1.7% day⁻¹). The highest levels of SGR, RNA/DNA and AA were detected in small (50–150 g) octopuses reared at 20 and 25 °C and in large (500–750 g) animals reared at 15 °C. Similar RNA/DNA levels and fatty acid percentages were found in wild octopuses. It is concluded that RNA/DNA, DHA, EPA and AA could be used as biochemical indices for predicting the growth rate of O. vulgaris.     

Changes in lipid class and fatty acid composition of adult male Litopenaeus vannamei (Boone) in response to culture temperature and food deprivation

The effects of culture temperature and food deprivation on lipid class and fatty acid composition of adult male Litopenaeus vannamei (Boone) were investigated. Shrimp were maintained in recirculating seawater systems at temperatures of 26 and 32°C and fed 75% dry commercial feed and 25% fresh‐frozen squid for 42 days. Additionally, groups of fed and non‐fed shrimp were maintained at 26°C for 17 days. In shrimp fed at either 26 or 32°C, polar lipids were the main constituents of total identified lipid classes in muscle tissue (66–71%), while neutral lipids were more abundant in hepatopancreas (82–88%). Higher levels of triglycerides were observed in lipids of shrimp hepatopancreas kept at 32°C, but no other lipid class was affected by temperature. A significantly higher proportion of 22:6n‐3 was consistent in muscle and hepatopancreas polar and neutral lipids of shrimp maintained at 26°C. In response to food deprivation, the amount of polar lipids, but not neutral lipids, was reduced by approximately 28% in muscle tissue, whereas all lipid reserves were almost depleted in the hepatopancreas. The variable consumption of some individual fatty acids was observed in polar and neutral lipids of both tissues.     

Effect of the interaction between body weight and temperature on growth and maximum daily food intake in sharpsnout sea bream (<Emphasis Type="Italic">Diplodus puntazzo</Emphasis>)

In experimental culture conditions in tanks, the effect of weight (W: 11–452 g) and temperature (T: 14–29°C) on the growth rate (SGR, % bw day⁻¹) and maximum daily food intake (SFR, % bw day⁻¹) in sharpsnout sea bream (Diplodus puntazzo) was studied. The possible combined effect of both independent variables (W and T) was also analyzed by multiple regression analysis, fitting the data to the equation Ln Y = Ln a + b Ln W + cT + dT ² + eT Ln W. Both SGR and SFR, and therefore feed efficiency (FE = SGR/SFR), were significantly influenced by the interaction between temperature and weight and may be expressed by means of the following equations: Ln SGR = −6.1705 + 0.5809T − 0.0087T ² − 0.0249T Ln W ( R_\textadj² R_{\text{adj}}^{2}  = 0.949; ANOVA P < 0.0001); Ln SFR = −4.8257 + 0.4425T − 0.0063T ² − 0.0163T Ln W ( R_\textadj² R_{\text{adj}}^{2}  = 0.964; ANOVA P < 0.0001).The results suggest that the optimum temperature for SGR and FE (T _SGRopt and T _FEopt), and the temperature at which the maximum SFR (T _SFRmax) is reached, decreases with body weight, in accordance with the equations: T _SGRopt = 33.297 − 1.435 Ln W; T _FEopt = 29.332 − 1.890 Ln W; and T _SFRmax = 34.941 − 1.304 Ln W, respectively. In this way, T _SGRopt is 28.4, 26.7, and 24.7°C; T _SFRmax is 30.5, 28.9, and 27.1°C and T _FEopt is 22.9, 20.6, and 18°C for 30, 100 and 400 g body weight, 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.     

Effect of different chilling rates for cold anaesthetization of Penaeus monodon (Fabricius) on the survival, duration and sensory quality under live storage in chilled sawdust

The present work was carried out with a view of determining the chilling rates for cold anaesthetization and live storage of Penaeus monodon (Fabricius) in chilled sawdust, for live transportation. Three chilling rates of 1.38 ± 0.16 °C h^?1 within 8 h (slow), 2.76 ± 0.32 °C h^?1 within 4 h (moderate) and 5.52 ± 0.64 °C h^?1 within 2 h (fast) were tested to cold anaesthetize 144 farm‐raised P. monodon (22–25 g) in each chilling rate at 15 g L^?1 salinity, from 25 °C down to 14 ± 1 °C in plastic net boxes kept in a refrigerated chilling tank provided with aeration. Eight cold‐anaesthetized shrimps subjected to each chilling rate were packed in an insulated cardboard box (triplicate) between two layers of moist and chilled (2–3 °C) sawdust, and kept inside a chilled storage cabinet at 14 ± 1 °C for durations of 16, 20, 24, 28, 32 and 36 h. Survival was determined by revitalizing the shrimps in aerated water with an initial temperature of 20 °C, which was raised to 28 ± 1 °C at 2.7 °C h^?1 within 3 h. Statistically valid, safe durations for obtaining 100% survival were 22.9 ± 1.1, 19.1 ± 0.4 and 14.6 ± 1.1 h, using probit analysis at the slow, moderate and fast chilling rates respectively. The weight loss (1.5–8.8%) due to cold anaesthetization and subsequent revitalization of the packed shrimp was insignificant. Sensory evaluation showed significant improvement in general appearance, and also in colour as well as in flavour of the meat when compared with that of the freshly harvested dead shrimps. The texture as well as odour of the raw and cooked meat between treated and untreated shrimps was unaffected. The effects of chilling rates and shipping durations on sensory quality were insignificant. One hundred per cent survival was obtained for 24, 20 and 16 h for the slow, moderate and fast chilling rates respectively. Percentage survival of the shrimps at different durations was significantly different among the chilling rates, but pair‐wise comparison revealed that the slow and moderate chilling rates were identical. Hence, the moderate chilling rate, which took only 4 h, can be considered the optimum, though the choice of different chilling rates depends on the duration of live storage desired.     

Induction of moulting in hatchery‐reared mangrove crab Scylla serrata juveniles through temperature manipulation or autotomy

The effects of temperature and autotomy of chelipeds on survival, growth and moulting of mangrove crab (Scylla serrata) juveniles were investigated under laboratory conditions for 60 days. Hatchery‐produced crabs with 2.0–2.3 cm internal carapace width (1.7–2.2 g body weight) at intermoult stage were exposed to one of four temperature treatments (constant 29, 32 or 35°C, or ambient [24–31°C]) or subjected to cheliped autotomy. All crabs held at 35°C had 100% mortality due to incomplete moulting during first moult. The mean survival of crabs at termination was 58%, 64% and 50% for ambient temperature, 29 and 32°C respectively. Specific growth rate (SGR) of crabs in the ambient and 29°C were comparable but significantly lower than those at 32°C. The moult interval of the crabs was significantly shorter in treatments with constant water temperature of 29 and 32°C compared with ambient temperature. The survival of crabs with intact chelipeds was comparable with those with one or two autotomized chelipeds. Crabs with intact or one autotomized chelipeds had significantly higher SGR than crabs with both chelipeds autotomized in the first moult. On the second moult, however, high SGR was observed in crabs with two chelipeds autotomized. The moult interval was significantly shorter in the autotomized crabs compared with crabs with intact chelipeds. The results suggest that the optimum water temperature for rearing S. serrata juveniles ranges from 29 to 32°C. Likewise, autotomy of chelipeds can promote moulting without adversely affecting survival of crabs.     

Temperature-dependent pharmacokinetics and tissue distribution of oxolinic acid in sea bass, Dicentrarchus labrax L., after a single intravascular injection

The pharmacokinetics and tissue distribution of oxolinic acid following an intravascular administration (15 mg kg^?1 fish) were determined in sea bass, Dicentrarchus labrax L. (110 g), at 13 °C and 22 °C water temperature. The kinetic profile of the drug was found to be temperature dependent, with increased temperature having a greater effect on distribution after equilibrium and the elimination phase than on the distribution process. The distibution half‐life of oxolinic acid was 1.15 and 2.76 h at 22 °C and 13 °C respectively, whereas the elimination half‐life of the drug was 55 h at 22 °C and 315 h at 13 °C. The values of the apparent volume of distribution (1.44 L kg^?1 at 22 °C and 3.31 L kg^?1 at 13 °C) and the volume of distribution at steady state (5.2 and 14.7 L kg^?1 at the high and low temperature respectively) were considerably different between the two tested temperatures. The total body clearance of the antibiotic was found to be low (1.47 L kg^?1 day^?1 at 22 °C and 0.80 L kg^?1 day^?1 at 13 °C). Lower rates of elimination were found for the liver compared with muscle, the difference increasing with increasing temperature, while elimination rates from the serum were higher than those of other tissues, especially at the high temperature.     

Probabilities of Low Nighttime Temperatures during Stocking and Harvest Seasons for Inland Shrimp Culture

Litopenaeus vannamei is cultured in earthen ponds at southern US inland sites when water temperatures permit shrimp survival and growth. The probability of a minimum air temperature ≤14 C for one, three, or five consecutive days at one coastal and eight inland sites where L. vannamei is or could be grown in ponds is high (50%) from late March through late April at all sites except Arcadia, Florida, and Harlingen, Texas. Probabilities are 10% by early May to early June. In the autumn, the 10 and 50% probability levels are reached in early‐ to mid‐September and by late September to mid‐October, respectively. Arcadia, Florida, and Harlingen, Texas, have the longest periods with low probabilities and Pecos, Texas, has the shortest periods. The maximum pond water temperature from the previous afternoon and the minimum air temperature from that night predicted the minimum pond water temperature the following morning for Pine Bluff, Arkansas: (R² = 0.886): T_min = 1.464 + 0.169A_min + 0.727T_max, where T_min = minimum daily pond water temperature (C), A_min = minimum air temperature (C) for the same day, and T_max = maximum pond water temperature (C) from the previous day. Pond stock out and harvest decisions can be guided by minimum air temperature probabilities and predicted water temperature.     

Effects of total ammonia,temperature and salinity on the mortality and viral replication of WSSV‐infected Chinese shrimp (Fenneropenaeus chinensis)

In this study, we evaluated the effects of three factors, total ammonia, temperature and salinity, on the mortality of and viral proliferation in white spot syndrome virus (WSSV)‐infected Chinese shrimp. Shrimp maintained in 30‰ seawater at 25°C with 0.34 mg L^?1 total ammonia (control group) were injected with approximately 20 WSSV particles per shrimp and subsequently subjected to the following conditions: 30‰ seawater at 25°C, with 6 mg L^?1 (N1 group) or 14 mg L^?1 (N2 group) total ammonia; 30‰ seawater at 18°C (T1 group) or 30°C (T2 group), with 0.34 mg L^?1 total ammonia and 20‰ (S1 group) or 40‰ (S2 group) seawater at 25°C, with 0.34 mg L^?1 total ammonia. An anova analysis revealed that the cumulative mortality of WSSV‐infected Chinese shrimp was significantly lower when reared in the T1 group compared to that of the T2 and control group. Similarly, the mortality of the shrimp in the S1 group was also significantly lower than that of the S2 and control group. No significant differences were detected among the N1, N2 and control groups. Accordingly, the WSSV level in the T1 and S1 groups was significantly lower than those in the control, T2 or S2 groups respectively. No significant differences in viral loads were detected among the control, N1 and N2 groups. The transfer of Chinese shrimp to lower temperature and lower salinity enhanced their resistance to WSSV infection, whereas a change in the concentration of total ammonia had no significant effect on the mortalities and viral loads of WSSV‐infected shrimp.     

Effects of temperature on food consumption, growth and oxygen consumption of freshwater prawn Macrobrachium rosenbergii (de Man 1879) postlarvae

Effects of temperature on food consumption, growth and oxygen consumption were estimated for the freshwater prawn Macrobrachium rosenbergii postlarvae at 23 °C, 28 °C and 33 °C in the laboratory. The results showed that the animal's initial body weight had a close linear relationship with food consumption and growth. Food consumption increased directly with temperature. Consumption rates (C; mg day^?1 ind^?1 ) of the 28 °C and 33 °C groups were much higher than that of the 23 °C group (P < 0.001), and the 33 °C group's consumption rate was higher than that of the 28 °C group (P < 0.05). The relationship of food consumption with temperature and initial body weight (W; mg) could be described as: C = 0.0679W + 0.185t? 3.17. Growth increased significantly with increased temperature. The relationship among specific growth rate, temperature and initial body weight was as follows: SGR = ?0.110W + 0.213t + 0.176. However, temperature showed no effect on growth efficiency. Oxygen consumption increased significantly with temperature (P < 0.01). The weight‐specific oxygen consumption rates (mg O₂ g^?1 h^?1) at 23 °C, 28 °C and 33 °C were 0.83, 1.16 and 1.49 mg O₂ g^?1 h^?1 for 61.92 mg M. rosenbergii.     

The growth and carbon allocation of abalone (Haliotis discus hannai) of different sizes at different temperatures based on the abalone‐kelp integrated multitrophic aquaculture model

The integration of shellfish and seaweed is an important and successful IMTA model. The IMTA of abalone and kelp has been well‐practiced in Sanggou Bay, China. In the present study, the growth and carbon allocation of abalone (Haliotis discus hannai) of different sizes (S, small; M, medium; L, large) fed kelp (Laminaria japonica) were investigated at different temperatures (10, 14, 18 and 22°C). A two‐way ANOVA showed that both size and temperature significantly affected the specific growth rate (SGR), food consumption (FC), feed conversion ratio (FCR) and apparent digestion rate (ADR) of abalone (p < 0.05), and significant interactions between the two factors were detected (p < 0.05). Curve estimation showed a significant quadratic relationship between SGR and temperature in each size class (p < 0.05). The two‐way ANOVA also showed that both size and temperature significantly affected all the measures of carbon allocation (p < 0.05) except for the carbon lost in metabolism (p > 0.05). All the measures of carbon allocation increased with the increasing temperature. It was concluded that it was better to culture H. discus hannai with a body weight less than 15 g at 20–22°C, and more than 15 g at 15–20°C to achieve good growth. The growth carbon of kelp around the abalone farm should be more than the metabolic carbon expenditure, which means the growth of kelp around the abalone farm should be more than 23.06%–61.91% of food consumption to maintain a carbon sink IMTA system without any carbon release.     

Live transportation of Macrobrachium rosenbergii (De Man) in chilled sawdust

Three cooling rates of 1.26±0.09°C h^?1 within 8 h (slow, T₁), 2.52±0.18°C h^?1 within 4 h (moderate, T₂) and 5.04±0.36°C h^?1 within 2 h (fast, T₃) were tested to cold‐anaesthetize farm raised Macrobrachium rosenbergii (De Man) (45–52 g) in each case from 25°C down to 15±1°C in a refrigerated chilling tank, provided with aeration. The cold‐anaesthetized prawns subjected to each chilling rate were packed in an insulated cardboard box (triplicate) between two layers of moist and chilled (2–3°C) sawdust, and kept inside a chilled storage cabinet at 15±1°C, for set durations of 6, 9, 12, 15 and 18 h. Survival was determined by revitalizing the prawns in aerated water with an initial temperature of 20°C, which was raised to 29±1°C within 3 h. The experiment was repeated using berried females acclimated to brackishwater of 12 g L^?1 salinity and the percentage survival recorded after live storage for durations ranging from 6 to 24 h at intervals of 3 h. Statistically valid safe durations for obtaining 100% survival of the cold anaesthetized and live stored prawns were determined using probit analysis at the three chilling rates tested, and were found to be 7.39, 6.98 and 4.54 h in the case of adult prawns, and 7.87, 8.17 and 6.43 h for berried females for T₁, T₂ and T₃ respectively. For practical purposes, the durations that yielded 95% survival rates were computed to be 16.47, 12.14 and 8.35 h in the case of adult prawns and 18.49, 19.02 and 11.11 h for berried females for T₁, T₂, and T₃ respectively. The berried prawns revitalized after live storage were incubated in tanks and the zoea larvae reared up to postlarvae (PL‐5), and compared against a control. No significant difference was found in larval hatch fecundity, survival rate and the production of PL L^?1 between the treatment and control, indicating that the method of cold anaesthetization and live storage of berried prawns could be used for successful transportation of broodstock.