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1.
One of the most severe impacts of urbanization on aquatic systems is the increasing presence of low oxygen environments caused by anthropogenic sources of pollution. As urbanization increases nationally and globally, it is becoming exceedingly important to understand how hypoxia affects aquatic fauna, especially fish species. In an effort to better understand the impacts of prolonged hypoxia on fishes, largemouth bass were held at 3.0 and 9.0 mg L?1 for 50 days, which has previously shown to be temporally sufficient to impart plastic phenotypic changes. Following the holding period, fish from each group were subjected to a low dissolved oxygen (DO) challenge of 2.0 mg L?1 for 6 h, and their physiological and hematological parameters were compared with control fish held for 6 h with no change in DO. There were no differences in the physiological stress responses between the two holding groups; however, the low oxygen holding group had increased hemoglobin and hematocrit levels following the 6-h low oxygen challenge compared with the high oxygen group. These results suggest largemouth bass exposed to chronic low oxygen conditions, either naturally or anthropogenically, may possess a beneficial advantage of increased oxygen uptake capacity during periods of low oxygen.  相似文献   

2.
The behavioural and metabolic responses of the largemouth bass Micropterus salmoides (Lacépède) to temperature were determined to define optimal thermal conditions. The final preferendum of largemouth bass juveniles determined with acute and gravitation methods was independent of the method (29.0–28.1 °C). The displacement velocity in the horizontal thermal gradient of bass juveniles was 22.4 cm h−1 in the light phase and 22.6 cm h−1 in the dark phase. Oxygen consumption rates in the largemouth bass increased significantly (P<0.05) from 48.8 to 69.4 mg O2 Kg−1 h−1 with an increase in the acclimation temperature from 20 to 33 °C. The temperature quotient (Q10) in the juveniles was 1.37–2.00 in the range of acclimation temperatures of 26–29 and 29–32 °C. The optimum temperature range for growth calculated using Jobling's equation was 28.1–28.6 °C and for Q10 values 26–29 °C. The results are discussed in relation to the use of this information in aquaculture.  相似文献   

3.
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   

4.
The metabolic physiological response to body mass, temperature (12–28 °C) and salinity (20–36 g L?1) was examined in this paper. Oxygen consumption rate, which is dependent on environmental conditions, was exponentially related to body mass and varied from 0.045 to 1.11 mg h?1 g?1. Oxygen consumption rate increased as salinity increased from 20 to 36 g L?1, and increased with increasing temperature. The effect of temperature gradient between experimental treatments on oxygen consumption rate was evaluated by calculating Q10 (the Arrehenius relationship for increase with temperature). The Q10 value within the temperature range from 12 to 16 °C was much higher than the value within the temperature range from 16 to 20 °C, 20 to 24 °C and 24 to 28 °C, indicating a reduced temperature dependence of ascidian metabolism at a high temperature.  相似文献   

5.
The objective of this study was to determinate the lethal concentration of dissolved oxygen (DO) over 96 hours of exposure (LC50–96h) for diploid and triploid jundia Rhamdia quelen juveniles. Diploid and triploid fish weighing approximately 4 g were subjected to DO concentrations varying between 0.4 and 1.3 mg O2 L?1; water temperature was maintained at 27?°C and pH at 6.3. The LC50–96h for diploids of Rhamdia quelen was 0.535 mg O2 L?1, while the value obtained for triploids was 6% greater. These results demonstrated that triploids of Rhamdia quelen juveniles have greater sensitivity to hypoxia compared to diploids.  相似文献   

6.
Piaractus mesopotamicus juveniles (total length 12 ± 0.5 mm) were exposed to different concentrations of ammonia‐N (un‐ionized plus ionized ammonia as nitrogen), using the static renewal method at different temperature levels (15, 20 and 25°C) at pH 7. The 24, 48, 72, 96 h LC50 values of ammonia‐N in P. mesopotamicus juveniles were 5.32, 4.19, 3.79 and 2.85 mg L?1 at 15°C; 4.81, 3.97, 3.25 and 2.50 mg L?1 at 20°C; and 4.16, 3.79, 2.58 and 1.97 mg L?1 at 25°C respectively. The 24, 48, 72, 96 h LC50 values of NH3‐N (un‐ionized ammonia as nitrogen) were 0.018, 0.014, 0.013, 0.009 mg L?1 at 15°C temperature; 0.023, 0.019, 0.016 and 0.012 mg L?1 at 20°C; 0.029, 0.026, 0.018 and 0.014 mg L?1 at 25°C. The temperature increase from 15 to 25°C caused an increase of ammonia‐N susceptibility by 21.80%, 9.55%, 31.92% and 30.87%, after 24, 48, 72 and 96 h exposure respectively. Furthermore, we found that exposure of fish to ammonia‐N caused an elevation in total haemoglobin and blood glucose with an increase of 2 mg L?1 concentration. Ammonia levels tolerated, especially in different temperatures levels, have important implications for the management of aquaculture.  相似文献   

7.
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.  相似文献   

8.
The effects of acclimation temperature (15, 20, 25 °C) on routine oxygen consumption and post-exercise maximal oxygen consumption rates (MO2) were measured in juvenile shortnose sturgeon (Acipenser brevirostrum LeSueur, 1818). The routine MO2 of shortnose sturgeon increased significantly from 126.75 mg O2 h?1 kg?1 at 15 °C to 253.13 mg O2 h?1 kg?1 at 25 °C. The temperature coefficient (Q 10) values of the routine metabolic rates ranged between 1.61 and 2.46, with the largest Q 10 values occurring between 15 and 20 °C. The average post-exercise MO2 of all temperature groups increased to a peak value immediately following the exercise, with levels increasing about 2-fold among all temperature groups. The Q 10 values for post-exercise MO2 ranged from 1.21 to 2.12, with the highest difference occurring between 15 and 20 °C. Post-exercise MO2 values of shortnose sturgeon in different temperature groups all decreased exponentially and statistically returned to pre-exercise (resting) levels by 30 min at 15 and 20 °C and by 60 min at 25 °C. The aerobic metabolic scope (post-exercise maximal MO2-routine MO2) increased to a maximum value ～156 mg O2 h?1 kg?1 at intermediate experimental temperatures (i.e., 20 °C) and then decreased as the temperature increased to 25 °C. However, this trend was not significant. The results suggest that juvenile shortnose sturgeon show flexibility in their ability to adapt to various temperature environments and in their responses to exhaustive exercise.  相似文献   

9.
Bioassays in static water (mean ± SD; temperature, 20–22 C; pH, 8.2–8.4; alkalinity, 205 ± 10 mg/L CaCO3; total hardness, 220 ± 10 mg/L CaCO3) were used to determine median lethal concentrations (LC50) of un-ionized ammonia (NH3-N) for striped bass Moronc saxatilis and hybrid striped bass M. saxatilis × M. chrysops. The 96 h LC50 for striped bass was 1.01 ± 0.24 mg/L NH3-N3 and was significantly higher than the LC50 for hybrid striped bass (0.64 ± 0.05 mg/L NH3-N). The effects of sublethal ammonia were evaluated after fish were exposed for 96 h to 0.0, 0.25, or 0.5 mg/L NH3-N or to additional exposure to oxygen depleted water (about 2.0 mg O2/L). Plasma ammonia of striped hass did not change as sublethal ammonia increased, but exposure to oxygen depletion caused a decrease in plasma ammonia. In contrast, plasma ammonia of hybrid striped bass increased as environmental ammonia increased, and increased further after exposure to oxygen depletion. Plasma cortisol levels of striped bass were significantly higher and more variable than cortisol levels of hybrid striped bass; additional exposure to oxygen depletion increased this variability, but these responses may be due to the stress of handling and confinement. Mean differences also existed between species for hemoglobin and hematocrit, while differences in variability occurred for osmolality and oxygen depletion rates. Striped bass tolerated ammonia better than hybrid striped bass but were more susceptible than hybrid striped bass to the additional stress of oxygen depletion. Most changes in physiological characteristics were relatively independent of environmental ammonia, but they were affected by oxygen depletion challenge.  相似文献   

10.
Influence of nitrite on two fish species, Eurasian perch (Perca fluviatilis L.) and largemouth bass (Micropterus salmoides Lacépède), was assessed in two acute toxicity tests. In the first one, lethal concentrations (48hLC50) of nitrite were estimated at 11 mg l?1 NO2 ? for perch and 882 mg l?1 NO2 ? for bass. In the second test, fishes were exposed for 48 h to concentrations representing ¼ and ½ value of 48hLC50 for each species. This test showed that the higher nitrite concentration in the water the higher methaemoglobin content in the blood, and nitrite levels in the blood plasma were observed in both species. On the other hand, leucocyte count showed opposite trend. Activity of NADH-methaemoglobin reductase was markedly lower in largemouth bass compared to Eurasian perch and was stimulated by nitrite exposure in neither of the species.  相似文献   

11.
It has been reported that metabolic rates of striped bass Morone saxatilis and hybrid striped bass M. chrysops♀ x M. saxatilis♂ are different. A series of experiments were conducted to further characterize oxygen consumption and metabolism of striped bass and its hybrid, the sunshine bass. Oxygen consumption was measured to determine standard and routine metabolic rates of striped bass and hybrid striped bass in a freshwater, flow‐through tank system. Additionally, blood chemistry stress indicators of the two bass groups were compared in both fresh and brackish water. Hematocrit (% PCV) and hemoglobin were measured in order to compare oxidative efficiencies of the bass. Plasma glucose, chlorides, and cortisol levels were measured to compare the relative stress status of the two bass types reared under experimental conditions. No significant differences were found in average daily oxygen consumption between striped bass and sunshine bass for either standard metabolism (P= 0.92), or routine metabolism (P = 0.86). Standard metabolic rates of oxygen consumption were 69 ± 4.1 and 68 ± 3.5 mg 02/kg3/4 bw/h for sunshine bass and striped bass respectively. Routine metabolic rates were 132 ± 30 and 125 ± 30 mg O2/kg3/4 bw/h for sunshine bass and striped bass respectively. While there were no significant differences in oxygen consumption between species, normal feeding activity generally resulted in increased oxygen consumption by the fish. Striped bass had significantly lower hematocrit values (P= 0.0001), but significantly higher hemoglobin concentrations than sunshine bass maintained in freshwater (P= 0.0001). Striped bass had significantly higher (P= 0.0001) levels of plasma glucose compared to sunshine bass (176 ± 8.6 vs. 103 ± 5.6 mg/dL respectively). Plasma chloride levels for striped bass (123 ± 1.9 mEq/L) were significantly higher (P= 0.041) than plasma chloride levels of sunshine bass (117 ± 1.7 mEq/L). Plasma cortisol levels were significantly higher (P= 0.0081) for striped bass (147 ± 8.4 ng/mL) compared to sunshine bass (119 ± 5.6 ng/ mL) when reared in freshwater. When maintained in brackish water, sunshine bass had significantly higher hematocrit values (P= 0.0001), and hemoglobin concentrations (P= 0.0012) when compared to striped bass. However, sunshine bass had significantly higher hemoglobin concentrations (P= 0.0012) when compared to striped bass. In addition, plasma glucose levels were significantly lower (P = 0.0079) for sunshine bass (79 ± 4.1 g/dL) when compared to striped bass (115 ± 11 g/dL). There were no significant differences between the bass in levels of chlorides or cortisol. No differences were detected in oxygen consumption. However, hybrid striped bass may have more efficient oxidative metabolism due to elevated hemoglobin concentrations. While striped bass hemoglobin values tended to be higher in brackish water than in freshwater, sunshine bass hematocrit or hemoglobin values generally were significantly higher than striped bass in both fresh and brackish water. Based on these results, hybrid striped bass may be capable of directing more energy towards growth than striped bass due to more efficient oxidative metabolism and lower losses of energy related to increased stress.  相似文献   

12.
Conditions for the induction of triploidy with cold shock of fertilized eggs of the spotted sand bass Paralabrax maculatofasciatus (Steindachner) were investigated. Different temperatures (12, 8 and 4 °C), timing of cold shock application (5, 10 and 15 min after fertilization) and duration of the shock (5, 10, 15 and 20 min) were tested. Triploidy was determined using flow cytometry at 12 h after larvae hatched. Triploids were produced only when the cold shock treatment was applied 5 min after fertilization. No significant difference was observed in the percentage of triploidy between temperature and the shock duration. At 8 and 4 °C, 100% triploidy was obtained at different durations of cold shock. Survival was significantly lower at 12 or 4 °C than at 8 °C. No significant difference was observed for shock duration at the temperature of 8 or 12 °C; however, at 4 °C, survival was significantly lower at longer durations. We recommend induction of triploidy by applying cold shock at 8 °C for a duration of 15–20 min starting at 5 min after fertilization, in the spotted sand bass.  相似文献   

13.
Largemouth bass virus (LMBV) is a recently discovered iridovirus that causes a fatal disease of largemouth bass, Micropterus salmoides (Lacepède). Fish can become infected by waterborne LMBV, but oral transmission of this virus has not been demonstrated previously. Largemouth bass were gavaged with guppies, Poecilia reticulata Peters, which had been injected with LMBV, and then sampled periodically during a 7‐week observation period. The dose of LMBV averaged 105.6 tissue culture infectious doses – 50% cytopathic endpoint (TCID50) per largemouth bass. Five of 24 largemouth bass exposed to LMBV became infected with the virus, but none of the fish had clinical signs typical of LMBV disease. Virus titres in largemouth bass were highest in swim bladder (105.5–9.5 TCID50 g?1) and were 105.2 TCID50 g?1 or lower in cutaneous mucus, head kidney, trunk kidney, spleen, gonad and intestine. These results indicate that LMBV can be transmitted orally to largemouth bass, but further study is needed to determine the factors affecting pathogenicity of the virus.  相似文献   

14.
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   

15.
This study aimed to evaluate the tolerance of common snook Centropomus undecimalis larvae and juveniles exposed to acute concentrations of un-ionized ammonia for 96 h at 35g L?1 salinity, after 24 h starvation. For that, 10 larvae (20.85 ± 1.46 mm) of 47 days post hatch (DPH) per experimental unit (1.5 L) were exposed to 0.00 ± 0.00, 0.65 ± 0.04, 1.29 ± 0.09, 2.59 ± 0.18, 3.88 ± 0.27, 5.17 ± 0.34, and 6.47 ± 0.43 mg L?1 NH3, in triplicates, at 26.72 ± 0.08°C, dissolved oxygen at 5.72 ± 0.10 mg L?1 and pH 8.45 ± 0.06. During this period, no mortalities were observed. Another trial was performed with five juveniles (20.35 ± 6.10 g, 13.90 ± 1.75 cm) per experimental unit (60 L) exposed to 0.00 ± 0.00, 2.26 ± 0.07, 2.68 ± 0.11, 3.20 ± 0.13, 3.68 ± 0.17, and 4.27 ± 0.16 mg L?1 NH3, in triplicates, at 21.90 ± 0.76°C, dissolved oxygen at 6.27 ± 0.21 mg L?1 and pH at 8.38 ± 0.04. Fish mortality increased as ammonia concentrations increased at each day, and LC50 96 h was 3.52 mg L?1 NH3. Larvae were less sensitive than juveniles, demonstrating that the environmental toxicity of ammonia to common snook is influenced by age. Sublethal exposition to ammonia caused histological damages in gills of common snook juveniles and variation on glucose levels, hematocrit, and red blood cells number, showing negative effects on fish homeostasis. Moreover, compared to other species, the common snook has great resistance to ammonia.  相似文献   

16.
The effect of irradiance and temperature on the photosynthesis of two Japanese agarophytes, Gelidium elegans and Pterocladiella tenuis (Gelidiales), was determined using dissolved oxygen sensors and pulse amplitude modulated (PAM) fluorometry. Gross photosynthesis and dark respiration rates were determined over a range of temperatures (8–36 °C). The highest gross photosynthetic rates were 40.3 and 37.0 mg O2 g ww ?1  min?1 and occurred at 24.3 and 25.5 °C [95 % Bayesian credible interval (BCI) 20.7–28.0 and 23.4–28.3 °C], respectively. The dark respiration rate in G. elegans and P. tenuis increased with increasing temperature at a rate of 0.10 and 0.31 mg O2 g ww ?1  min?1 °C?1 , respectively. Modeling the net photosynthesis–irradiance (P–E) responses of G. elegans and P. tenuis at 20 °C revealed that the net photosynthetic rates quickly increased at irradiance levels below the estimated saturation irradiance of 88 and 83 µmol photons m?2 s?1, with a compensation irradiance of 14 and 19 µmol photons m?2 s?1, respectively. The highest value of the maximum effective quantum yield (Φ PSII) occurred at 20.1 °C (BCI 18.9–21.5 °C) and 21.3 °C (BCI 20.2–22.5 °C) for G. elegans and P. tenuis and was 0.49 and 0.45, respectively. These optimal temperatures of Φ PSII were relatively lower than those determined by the photosynthesis–temperature model of oxygen evolution. The temperature response of these species indicates that they are probably well adapted to the current range of seawater temperatures in the study site but that they are near the boundary of their tolerable limits.  相似文献   

17.
Oxygen demand by all animals is driven primarily by their needs for sustaining metabolism. Typically, larger animals require more oxygen and cellular fuel to carry out respiration than smaller animals. This relationship in most cases is not linear and is usually described by a coefficient and exponent (e.g. axb): the exponent b showing the relationship between live‐weight and energy/oxygen demand and is often termed the metabolic body weight (MBW) exponent, while the coefficient (a) tends to be temperature specific and describes the relationship between MBW and maintenance metabolic energy and oxygen demand at that specific temperature. Across all temperatures (range 26.0–32.0°C), the relationship between barramundi (Lates calcarifer) live‐weight (x; g) and relative oxygen consumption as standard metabolic rate (y; mg O2 kg?1 h?1) at 29.4±1.5°C (mean±SD) was described by the exponential curve: y=710.19 x?0.3268, R2=0.6875 (n=222 assessments). Examination of the same data but on a gross oxygen consumption (mg O2 h?1) basis showed a relationship between live‐weight (x; g) and gross oxygen consumption (y; mg O2 h?1) that was described by the exponential curve: y=0.710 x0.6732, R2=0.9033. Evaluation of the combined relationship between fish live‐weight (y; g) and water temperature (x; °C) on gross oxygen consumption rate (z; mg O2 h?1) was described by the equation: z=(?20.7818+1.4017x?0.0227x2) ×y0.673.  相似文献   

18.
Summer stratification often leads to large areas of hypolimnetic hypoxia in lakes and reservoirs. These areas of hypoxia alter fish behaviours and distributions as well as restrict access to valuable prey resources, yet few studies have examined foraging behaviour of fish in response to low dissolved oxygen (DO) concentrations. We observed foraging behaviour of juvenile largemouth bass, Micropterus salmoides, in response to varying DO concentrations in tanks that simulated a stratified lake water column during the summer: 28°C oxygenated epilimnion, 15°C deoxygenated hypolimnion. Compared with saturated concentrations (8.0–9.0 mg/L), hypolimnetic oxygen concentrations of 3.0 mg/L and 1.5 mg/L resulted in a drastic decrease in prey consumption, handling efficiency and time spent below the thermocline mainly due to avoidance behaviour of hypoxic conditions. However, we found at high hypolimnetic prey densities, individual fish were more willing to venture into reduced oxygen concentrations. Several unique behaviours including transporting prey above the oxycline for consumption, aquatic surface respiration and gill flaring were employed by largemouth bass foraging in low oxygen environments. Reduced hypolimnetic oxygen concentrations may influence and alter feeding strategies, especially for fish that rely on benthic prey resources.  相似文献   

19.
The effects of temperature on resting oxygen consumption rate (MO2rest) and excess post-exercise oxygen consumption (EPOC) after exhaustive exercise (chasing) were measured in juvenile southern catfish (Silurus meridionalis) (8.40 ± 0.30 g, n = 40) to test whether temperature has a significant influence on MO2rest, maximum post-exercise oxygen consumption rate (MO2peak) and EPOC and to investigate how metabolic scope (MS: MO2peak − MO2rest) varies with acclimation temperature. The MO2rest increased from 64.7 (10°C) to 160.3 mg O2 h−1 kg−1 (25°C) (P < 0.05) and reached a plateau between 25 and 30°C. The post-exercise MO2 in all temperature groups increased immediately to the peak values and then decreased slowly to a steady state that was higher than the pre-exercise MO2. The MO2peak did not significantly differ among the 20, 25 and 30°C groups, though these values were much higher than those of the lower temperature groups (10 and 15°C) (P < 0.05). The duration of EPOC varied from 32.9 min at 10°C to 345 min at 20°C, depending on the acclimation temperatures. The MS values of the lower temperature groups (10 and 15°C) were significantly smaller than those of the higher temperature groups (20, 25 and 30°C) (P < 0.05). The magnitude of EPOC varied ninefold among all of the temperature groups and was the largest for the 20°C temperature group (about 422.4 mg O2 kg−1). These results suggested that (1) the acclimation temperature had a significant effect on maintenance metabolism (as indicated by MO2rest) and the post-exercise metabolic recovery process (as indicated by MO2peak, duration and magnitude of EPOC), and (2) the change of the MS as a function of acclimation temperature in juvenile southern catfish might be related to their high degree of physiological flexibility, which allows them to adapt to changes in environmental conditions in their habitat in the Yangtze River and the Jialing River.  相似文献   

20.
The direct impact of oxidation–reduction potential (ORP) on fish welfare and water quality in marine recirculating aquaculture systems (RAS) is poorly documented. In this study, the effects of the fish size (S1, S2, S3) and ORP level (normal, four successive levels) on the performance of European sea bass (Dicentrarchus labrax) were investigated. Three size fish were distributed into two RAS (RAS and RAS O3). Ozone was injected into RAS O3 to increase the ORP level. The ORP was stabilized to four successive levels: 260–300, 300–320, 320–350, and 300–320 mV in fish tanks during four periods (P1–4). At the last day of each period, the hematological parameters, plasma protein and mortality of sea bass were analyzed. Two-way ANOVA revealed that several hematological parameters, including pH, hematocrit, concentrations of oxygen, carbon dioxide, glucose (Glu), ionized calcium, kalium, and hemoglobin, were significantly influenced by the increased ORP levels over the experimental period. The alteration in blood Glu and plasma protein concentration showed that ORP around 300–320 mV started to stress sea bass. Once the ORP exceeded 320 mV in the tanks during the P3 period, mortality occurred even when total residual oxidants/ozone-produced oxidants was only 0.03–0.05 mg L?1 in the fish tanks. At the same time, plasma protein decreased notably due to appetite depression. After the decrease in ORP during the P4 period, mortality continued. In conclusion, the results strongly suggest that for European sea bass in RAS, the ORP should not exceed 320 mV in the tanks. Once ozonation damaged fish, the effect seemed to be irreversible. However, how ORP affected related hematological parameters still need the further investigations.  相似文献   

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