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1.
The effects of temperature, salinity, light intensity and pH on the growth and morphology of Chattonella marina (Subrahmanyan) Hara & Chihara were examined. Optimal growth was observed at temperatures of 20-25°C, salinities of 20-30%o, light intensities of 60-140 μE m?2 s_1 and pH 7.5-8.5. Growth did not occur at temperatures below 15°C or above 30°C, and at salinities below 10%o. The morphology (shape) of the cells was strongly affected by temperature. At 20°C and 25°C, the population occurred mostly in a spindle-like form, whereas at 10°C, 90% of the cells became spherical within 10 days of inoculation and stationary phase cultures consisted entirely of spherical cells. Morphology was also markedly affected at 30°C. The number of spindle-like cells was highest at 20-30%o and was less at lower salinities. Light intensity and pH did not influence morphology markedly under the range of light intensities (20-180 μE m ?2 s-?1) and pH (6.5-8.5) tested.  相似文献   

2.
The kuruma shrimp, Penaeus (Marsupenaeus) japonicus (Bate, 1888), is a valuable aquaculture species in Queensland, Australia. The shrimp is supplied live to the Japanese market and must survive emersed transport for up to 36 h. In-transit mortality after harvest from high water temperatures (> 30 °C) has been reported by the industry, and a knowledge of the effects of high water temperature may provide important information for producers on grow-out management, timing of production and farm location. Experiments were conducted to determine the effect of high water temperature on survival, moulting and food consumption in P. japonicus. Replicated groups of 15.6 ± 0.2 g shrimp were acclimated and exposed to five temperatures, between 28 and 36 °C, for up to 28 days. Mortality was highest at 36 °C and equally lowest between 28 °C and 32 °C. Intermoult period was not significantly different for temperatures between 28 and 32 °C (19.8–15.5 days) but was significantly greater above 32 °C (27.4 days at 34 °C and > 104 days at 36 °C). There was evidence of moulting synchrony at 28 °C. Mean daily food consumption was highest at 32 °C at 2.34% of body weight, but decreased to 1.56% at 28 °C and 1.33% at 36 °C. Over the range of water temperatures examined, survival, moulting rate and food consumption were highest at 32 °C.  相似文献   

3.
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.  相似文献   

4.
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.  相似文献   

5.
This paper reports on a 4 × 4 factorial design experiment conducted to examine the combined effects of temperature and salinity on embryonic development and growth and survival of black-lip pearl oyster, Pinctada margaritifera (L.) larvae. The temperatures used were 20 °C, 25 °C, 30 °C and 35 °C, and the salinities were 25°/oo, 30°/oo, 35°/oo and 40°/oo. Response surface contour diagrams were generated from the survival and growth data to estimate optimal conditions. Normal development of embryos occurred only from 25 °C to 30 °C. The optimal conditions for maximum survival and growth were 26–29 °C and 28–32°/oo. Temperatures of 35 °C or greater were lethal for larvae and, at all temperatures tested, larval growth and survival were lowest at a salinity of 40°/oo.  相似文献   

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

7.
Juveniles of gilthead sea bream, Sparus auratus L., with individual weight 1.92 g, were reared under salinities of 8, 18, 28 and 38%o. The transfer to lower salinities (8-28%o) was abrupt. The results showed that better daily growth rates and food conversion efficiencies (FCE) when growing at 28%o gave the best performance. Statistically, salinity values above 28%o do not significantly affect daily growth rates and daily voluntary food intake. Maintenance requirement decreases linearly with increasing salinity. In particular, a l%o decrease of salinity is associated with a 0.014 (% body weight day-1) increase of daily maintenance requirement. Mortality rates are high at salinities of 8 and 38%o (65% and 20% respectively) and minimal (1-3%) for fish reared under intermediate salinities (18-28%o). Finally, scope for growth, expressed as the minimum difference between food amount eaten and food attributed to growth, is better when the fish are kept at a salinity of 28%o. This means that most of the food amount eaten is attributed to growth and food wastage is minimal. These results confirm that gilthead sea bream fry show best performance when reared at a salinity of 28%o.  相似文献   

8.
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.  相似文献   

9.
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.  相似文献   

10.
The physiological responses of the juvenile Crassostrea nippona in terms of filtration, oxygen consumption and ammonia excretion to changes in temperature (16–32°C), salinity (15–35 psu) and body size (small, medium and large) were investigated. In this study, the values of filtration rate (FR), oxygen consumption rate (OCR) and ammonia excretion rate (AER) increased with temperature rising from 16°C to 24°C, reaching the highest values at 24°C and 28°C; with any further increase in temperature above this limit, these values decrease drastically (p < .05). The highest Q10 coefficients were 2.75 for large, 3.54 for medium at 16–20 and 3.47 for small size at 20–24°C respectively. Moreover, the responses of FR and OCR were found to be influenced significantly by salinity, tending to increase concomitantly with salinity up to 25–30 psu, though the values of these parameters were diminished dramatically (p < .05) above this level, showing a reverse pattern from that observed in AER, which firstly decreased to the lowest level at 25 and 30 psu, and then severely (p < .05) increased to the highest level at 35 psu. In addition, the low O:N ratios of all sizes of C. nippona at 16°C and 30–35 psu were indicative of a protein‐dominated catabolism, whereas the O:N ratios of large size at 20–32°C and all sizes at 20–30 psu, indicating that the metabolic energy from protein diminished and lipid and carbohydrate were used as the energy substrates. Physiological rates of C. nippona were well correlated with its size. The average values of mass exponents (b‐values) estimated in the present study were 0.657 for OCR and 0.776 for AER at different temperatures, and 0.647 for OCR and 0.767 for AER at varying salinities, signifying that physiological process of C. nippona becomes relatively slower with increasing body size regardless of temperature or salinity. Finally, our results confirm that the optimal temperature and salinity for juvenile C. nippona lie within 24–28°C and 25–30 psu respectively. The results of physiological traits in response to environmental factors of this species are informative in site selection for the cultivation.  相似文献   

11.
High larval mortalities during rearing of gilthead bream, Sparus auratus L., led to experiments on the influence of salinity and temperature on eggs and yolk-sac larvae. Test salinities ranged from 5 to 70 ppt for eggs and from 15 to 45 ppt for larvae; experimental temperatures were 18–20°C for eggs and 18, 23 and 26°C for larvae. Spawning conditions were 18–20°C and 33–35 ppt salinity; the yolk-sac larvae were chosen from hatches obtained under similar conditions (18°C and 35 ppt salinity). For eggs the optimum survival range was found to be 30–50 ppt at 18°C and 15–60 ppt at 23°C, while that for yolk-sac larvae was 15–25 ppt at all three temperatures. Choosing normal development (no dorsal curvature) as the decisive criterion, the optimum salinity range for egg incubation was reduced to 30–40 ppt at 18°C and to 35–45 ppt at 23°C, while that for the yolk-sac stage remained 15–25 ppt at all test temperatures. Egg incubation was most successful at salinity-temperature combinations close to those during spawning, whereas salinity had to be reduced by at least 10 ppt for yolk-sac larvae.  相似文献   

12.
Physiological responses of pink abalone Haliotis corrugata were determined under different temperature and salinity conditions. Oxygen consumption rate was not affected by temperature and salinity. Ammonium excretion of pink abalone was inversely related to salinity. The O:N ratio indicated that abalone maintained in lower salinities had an interval of 4.9–7.7, which is indicative of a protein‐dominated metabolism, whereas the O:N in 35‰ was 28.8–35.5 for both temperatures, suggesting that carbohydrates were used as energy substrate. Haemolymph osmolality of abalone exposed to 20 and 24 °C was slightly hyperiso‐osmoconformic in salinity ranges of 20–35‰. The results of this study suggested that for optimized culture, pink abalone should be cultivated at 24 °C at a salinity of 35‰.  相似文献   

13.
This study was performed to determine the growth and survival patterns of the juvenile yellowleg shrimp Farfantepenaeus californiensis cohabiting with the green feather alga Caulerpa sertularioides over a range of temperatures (18, 22, 25, 28 and 32°C) found throughout the year in the Gulf of California. From an initial weight of 46 ± 10 mg, shrimp cohabiting with green feather algae increased in weight by an average of 0.57 (±0.07), 5.44 (±0.45), 6.36 (±0.37), 7.66 (±0.26) and 5.96 (±0.59) g at 18, 22, 25, 28 and 32°C, respectively, whereas shrimp grown without seaweed increased in weight by an average of 0.28 (±0.026), 2.66 (±0.24), 3.15 (±0.49), 4.00 (±0.67), and 3.54 (±0.09) g respectively. Statistically significant differences were observed for the growth rates of juvenile yellowleg shrimp in the presence of C. sertularioides and peak growth was observed at 28°C in experiments with macroalgae. No significant differences were observed for shrimp survival except at 32°C without macroalgae, where survival was lower. These results suggest a beneficial and growth‐promoting effect of cohabitation with live C. sertularioides on F. californiensis.  相似文献   

14.
It is presumed that in hypo‐ and hypersaline environments, shrimp’s requirements for some specific nutrients, such as protein, may differ from those known in the marine habitat; however, few investigations have been conducted in this area of study. In the present investigation, the effects of salinity and dietary protein level on the biological performance, tissue protein, and water content of Pacific white shrimp, Litopenaeus vannamei, were evaluated. In a 3 × 4 factorial experiment, juvenile shrimp with an average initial weight of 0.36 ± 0.02 g were exposed for 32 d to salinities of 2, 35, and 50 ppt and fed experimental diets with crude protein contents of 25, 30, 35, and 40%. A significant effect of salinity on growth of shrimp was detected, with the growth responses (final weight, weight gain) ranked in the order 2 ppt (3.87, 3.50 g) > 35 ppt (3.40, 3.04 g) > 50 ppt (2.84, 2.47 g). No effects of dietary protein level or an interaction between salinity and protein on growth of shrimp were observed under the experimental conditions of this study. Percent survival of shrimp fed the highest protein content (40%, survival of 74%) was, however, significantly lower than those of shrimp fed the other feeds (25, 30 and 35% protein, survival of 99, 91, and 94%, respectively), a result likely associated with the concentration of total ammonia nitrogen, which increased significantly at increasing protein levels. Final water content of whole shrimp was significantly lower in animals exposed to 50 ppt (70.8%) than in shrimp held at 2 (73.7%) and 35 ppt (72.3%). No effect of salinity, protein, or their interaction was observed on the protein content of whole shrimp. The results of the present study are in agreement with reports of superior and inferior growth of L. vannamei reared in hypo‐ and hypersaline environments, respectively, as compared to what is generally observed in seawater.  相似文献   

15.
The respiratory rates of Tawny puffer Takifugu flavidus juvenile were measured at four temperatures (20, 23, 26 and 29 °C) and seven salinities (5, 10, 15, 20, 25, 30 and 35 g L?1). The results showed that both temperature and salinity significantly affected the oxygen consumption of tawny puffer juvenile. The oxygen consumption rate (OCR) increased significantly with an increase in the temperature from 20 to 29 °C. Over the entire experimental temperature range (20–29 °C), the Q10 value was 1.59, and the lowest Q10 value was found between 23 and 26 °C. The optimal temperature for the juvenile lies between 23 °C and 26 °C. The OCR at 25 g L?1 was the highest among all salinity treatments. The OCRs show a parabolic relationship with salinity (5–35 g L?1). From the quadratic relationship, the highest OCR was predicted to occur at 23.56 g L?1. The optimal salinity range for the juvenile is from 23 to 25 g L?1. The results of this study are useful towards facilitating an increase in the production of the species juvenile culture.  相似文献   

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

17.
The effects of incubation salinity on survival and morphological development of yolk sac larvae of Atlantic halibut, Hippoglossus hippoglossus (L.), were studied at two salinities, 35.5%o and 32.3%o. Yolk sac larvae incubated at 35.5%o developed early tail deformities before 50 day-degrees (9 days post-hatch), and necrosis, oedema and calculus in the urinary bladder at about 150 day-degrees (28 days post-hatch). However, the incidence and severity of mouth deformity was not influenced by salinity. The cumulative mortality up to first feeding was 17% when the larvae were incubated at 3 5.5%o compared to 7% at 32.3%o. A broad variation between the different larval groups was noted in the extent of injuries induced by the higher salinity. Therefore, salinity must be considered as a critical environmental parameter for the yolk sac larvae of Atlantic halibut in aquaculture.  相似文献   

18.
Shrimp farming at low salinity is a trend that will continue to grow globally. Performance of Litopenaeus vannamei postlarvae in the nursery at different salinities with a biofloc technology (BFT) system needs to be explored further, as the nursery is currently used as a transitional stage between the hatchery and grow-out ponds. Hence, this study evaluated the effect of seven salinity levels (2, 4, 8, 12, 16, 25, and 35 ‰) on the performance of L. vannamei postlarvae reared with a BFT system and zero-water exchange at 2000 org/m3. Additionally, this study evaluated the water quality of all salinity treatments. After 28 days of culture, the findings showed that, under biofloc conditions, salinity affected the performance of some variables of water quality in some cases, but only the combination of a high nitrite-N concentration (>4 mg/l) and low salinity (2 and 4 ‰) caused up to 100 % shrimp mortality in the first 2 weeks. In the rest of the treatments (8, 12, 16, 25, and 35  ‰), shrimp survival was >72 %. Shrimp mortality was affected by salinity, especially when it decreased from 35–25–16 to 12 and 8 ‰. The organisms reared at low salinities presented lower final weights and specific growth rate than those reared at higher salinities. An inverse relationship was shown between the ion concentration and the final weight of shrimp.  相似文献   

19.
SUMMARY: Effects of temperature, irradiation, salinity and inorganic nitrogen concentration on two cultured strains of zooxanthellae isolated from the corals Pocillopora damicornis (strain P) and Montipora verrucosa (strain M) were studied. Each strain showed different growth responses in terms of temperature and light intensity. A maximum growth rate of strain P, 1.2 per day, was observed at 32°C under all light intensities examined (5–40 μEm−2s−1). However, its photosystem 2 activity (FRI) was higher at 28°C than at 32°C under most light intensities. In contrast, the growth rate of strain M was affected more by light intensity and was almost invariably affected at all temperatures examined (24–36°C). Both algal strains had a comparable growth rate and FRI at salinities from 20 to 35 PSU under moderate temperature and irradiant conditions. High temperature and low irradiation reduced the algal tolerance against low salinity. The gross photosynthesis per cell was not affected by the ammonium enrichment more than 5 μM per day although the cellular chlorophyll a content and cell density increased in proportion with the ammonium enrichment up to 20 μM per day. A potential response of zooxanthellae to the multiple environmental stresses was shown from these results.  相似文献   

20.
The adaptive evolution of the Notothenia rossii occurred under the selective pressure of stable and low temperatures. It is an opportunistic feeder of Antarctic krill and the fluoride in the krill carapace is apparently not toxic. We investigated the interactive effect of fluoride, elevated temperatures, and low salinity on the plasmatic constituents of this Antarctic fish. The experiments were conducted at the Brazilian Antarctic Station Comandante Ferraz (EACF), located on King George Island. The Antarctic fish N. rossii was acclimatized to eight thermo-saline-trophic conditions, combining two temperatures (0 and 4 °C), two salinities (35 and 20), and two trophic conditions (with/without fluoride) for an 11-day period. Trophic fluoride was not able to alter the plasmatic levels of glucose, cholesterol, plasmatic protein, Cl?, Mg2+, Ca2+, and inorganic phosphate, but induced an acute elevation of triglycerides at 0 °C and salinity of 35. At low salinity, hyperglycemia, hypertriglyceridemia, and hypocalcemia were observed. The thermo-saline interaction at 4 °C was able to minimize the effects of fluoride and low salinity on the plasmatic constituents levels.  相似文献   

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