首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献，搜索用时 442 毫秒
1.
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.  相似文献   

2.
Abstract

Potassium deficient inland saline (10 g L?1 salinity) well water was supplemented with muriate of potash to achieve 50% (57 mg L?1) and 100% (114 mg L?1) of seawater potassium concentration and used for the production of tiger shrimp (Penaeus monodon). Total mortality was observed in non-supplemented water within 6 days compared to 88.0% survival in K+100% and 85.3% survival in K+50% up to 60 days. P. monodon were subsequently cultured for 110 days in two identical 0.25-ha ponds supplied with water of 10 g L?1 and supplemented with the potassium equivalent of 35% of seawater. Survival and production were 55.8% to 64.25% and 157.70 kg (630.8 kg ha?1) to 172.75 kg (691 kg ha?1), respectively.  相似文献   

3.
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.  相似文献   

4.
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.  相似文献   

5.
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   

6.
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   

7.
A 60‐d growth trial was conducted with the black tiger prawn, Penaeus monodon (ca. 0.8 g juveniles) at CIFE Rohtak Centre to evaluate the effects of salinity and Na+/K+ ratio of inland saline water on shrimp growth, survival, and osmoregulation. Three different salinities (5, 10, and 15 ppt) and five different Na+/K+ ratios (25:1, 45:1, 65:1, 85:1, and 27.9:1), for a total of 15 treatments were prepared by ionic manipulation. The medium with Na+/K+ ratio 27.9 was reconstituted seawater and was used as the reference treatment. At the end of the 60‐d trial both salinity and Na+/K+ ratio significantly influenced the survival and growth of shrimp in inland saline water (P < 0.05). Final mean individual weight, weight gain (%) (WG [%]) increased with decreasing Na+/K+ ratios. Survival rates were significantly higher (P < 0.05) for Na+/K+ ratio 45 and 27.9 at salinities 10 and 15 ppt, respectively. Minimum growth and survival (0–24%) were observed in mediums with Na+/K+ ratio 85 at all salinities. Serum osmolality and osmoregulatory capacity were similar across all treatments at identical salinities except for sodium to potassium ratio (Na+/K+) 85. The serum sodium and potassium levels did not show any significant difference (P > 0.05) for mediums with Na+/K+ ratio 25, 45, 65, and 27.9 at all salinities. Significantly different (P < 0.05) serum sodium levels were observed in mediums with Na+/K+ ratio 85 at all salinities at the end of the trial. The serum potassium levels were significantly low in treatments with Na+/K+ ratio 85. There was no significant difference in the serum magnesium levels between treatments and the serum calcium levels were significantly lower for shrimp reared in the reference mediums. Results of this study confirm that P. monodon can be successfully cultured in low salinity waters with Na+/K+ ratio ranging between 25 and 45:1.  相似文献   

8.
The brown shrimp, Farfantepenaeus californiensis (Holmes), is a species native to north‐west Mexico, where its culture potential is presently being addressed. Because of the climatic conditions prevailing in the region, salinities over 40 g L?1 is a commonly encountered problem. In the present study, the effect of salinity on the growth and mortality of juvenile F. californiensis is described. The change in short‐term routine metabolism at different salinities was also evaluated in order to define the adaptive capacity of the shrimp and to provide insight into the changes in the pathways of energy distribution. Groups of shrimp were exposed to increasing salinity (25, 35, 45 and 55 g L?1), and growth and survival rates after 75 days were determined in duplicate 1.8‐m3 tanks for each salinity level. Significant differences were found in final weight, growth rate and mortality of shrimp as a result of salinity level. Final mean shrimp weights at increasing salinity levels were 10.0, 9.4, 8.6 and 7.8 g. Corresponding mortality was 24.4%, 15.1%, 33.6% and 55.7%. Oxygen consumption was found to depend significantly on salinity and was equivalent to 0.0027, 0.0037, 0.0043 and 0.0053 mg g?1 min?1 respectively for the increasing salinities. The increased rate of oxygen consumption at high salinities reflects the response of the organism to osmoregulatory and ionic imbalances. Increased energy requirements to fulfil basic metabolic function as salinity increased resulted in a reduction in the energy that could be diverted to growth. Consequently, the culture of the brown shrimp at salinities over 35 g L?1 would probably result in reduced yields.  相似文献   

9.
The nitrite toxicity was estimated in juveniles of L. vannamei. The 24, 48, 72 and 96 h LC50 of nitrite‐N on juveniles were 8.1, 7.9, 6.8 and 5.7 mg L?1 at 0.6 g L?1; 14.4, 9.6 8.3 and 7.0 mg L?1 at 1.0 g L?1; 19.4, 15.4, 13.4 and 12.4 mg L?1 at 2.0 g L?1 of salinity respectively. The tolerance of juveniles to nitrite decreased at 96 h of exposure by 18.6% and 54.0%, when salinity declined from 1.0 to 0.6 g L?1 and from 2.0 to 0.6 g L?1 respectively. The safe concentrations at salinities of 0.6, 1.0 and 2.0 g L?1 were 0.28, 0.35 and 0.62 mg L?1 nitrite‐N respectively. The relationship between LC50 (mg L?1), salinity (S) (g L?1) and exposure time (T) (h) was LC50 = 8.4688 + 5.6764S – 0.0762T for salinities from 0.6 to 2.0 g L?1 and for exposure times from 24 to 96 h; the relationship between survival (%) and nitrite‐N concentration (C) for salinity of 0.6–2.0 g L?1, nitrite‐N concentrations of 0–40 mg L?1 and exposure times from 0 to 96 h was as follows: survival (%) = 0.8442 + 0.1909S – 0.0038T – 0.0277C + 0.0008ST + 0.0001CT–0.0029SC, and the tentative equation for predicting the 96‐h LC50 to salinities from 0.6 to 35 g L?1 in L. vannamei juveniles (3.9–4.4 g) was 96‐h LC50 = 0.2127 S2 + 1.558S + 5.9868. For nitrite toxicity, it is shown that a small change in salinity of waters from 2.0 to 0.6 g L?1 is more critical for L. vannamei than when wider differences in salinity occur in brackish and marine waters (15–35 g L?1).  相似文献   

10.
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.  相似文献   

11.
Larvae of Metapenaeus monoceros (Fabricius) at protozoea 1 (PZ1) stage were stocked in 2‐L glass flasks to investigate the effects of various salinities (25, 30, 35, 40, 45, 50 and 55 ppt) on growth and survival until the post‐larval (PL) stages. The PZ larvae were not able to tolerate a sudden salinity drop of over 10 ppt. Yet, an abrupt salinity increase of over 10 or even 15 ppt did not cause mortality. The PZ larvae were successfully acclimated to different test salinities at a rate of 4 ppt h?1. The larvae displayed better tolerance to high rather than low salinities. The lowest and highest critical salinities appeared to be 22 and 55 ppt respectively. Taking into account survival, growth and development results, the optimal salinity for the larval culture of M. monoceros inhabiting the Eastern Mediterranean was 40 ppt. At this salinity, the PZ1 larvae were successfully cultured until PL1 stage within 11 days with 68% survival on a feeding regime of Tetraselmis chuii Kylin (Butcher) (20 cells μ L?1), Chaetoceros calcitrans Paulsen (50 cells μ L?1), Isochrysis galbana Parke (30 cells μL?1) and five newly hatched Artemia nauplii mL?1 from M1 onwards at 28 °C.  相似文献   

12.
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   

13.
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.  相似文献   

14.
The suitability of inland saline groundwater as a medium to culture juvenile cobia, Rachycentron canadum, was assessed. In the first experiment, juvenile cobia stocked in raw (unamended) saline groundwater at salinities of 5, 10, and 15 g/L exhibited complete mortality after 108, 176, and 195 hr, respectively. The second experiment evaluated the rearing of juvenile cobia (mean weight ~9.23 ± 0.12 g) in potassium (K+)‐amended saline groundwater (100% K+ fortified) and reconstituted seawater at salinities of 5, 10, and 15 g/L to assess growth and osmoregulation in distinct culture media. Following 60 days of culture, all fish survived the experimental period. Final mean bodyweight of cobia reared in K+‐amended saline groundwater (103.2–115.8 g) and seawater (111.2–113.8 g) of different salinities did not vary significantly (p > .05). No differences (p > .05) were observed in specific growth rate, weight gain (%), and feed conversion ratio between treatment groups. Serum osmolality increased with salinity and was significantly higher (p < .05) for fish in K+‐amended saline groundwater (353–361 mOsmol/Kg) than in reconstituted seawater (319–332 mOsmol/Kg), although differences were not observed between salinities by water type. Cobia stocked in saline groundwater of different salinities were osmoregulating normally, and the higher values observed may be because of variations in ionic composition and other interfering ions in saline groundwater. Trial results suggest that juvenile cobia can achieve optimal growth in K+‐amended saline groundwater of low and intermediate salinities.  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.
Survival of marble goby larvae fed either Rhodovulum sulfidophilum, a phototrophic bacterium cultured from palm oil mill effluent (pPB), or microalgae ( Nannochloropsis sp.) was evaluated at two salinities. Larvae directly fed pPB had survival of 0–29% at 5 g L?1 salinity and 0–19% at 10 g L?1 salinity, whereas larvae directly fed microalgae suffered complete mortality after 20 days of culture at both salinities. However, larvae indirectly fed pPB or microalgae, i.e. via rotifers (Days 1–30) and Artemia nauplii (Days 21–30) cultured solely from pPB or microalgae, showed improved survival of 35–55% or 44–49% at 5 g L?1 salinity respectively. In all experiments, fish larvae reared at 5 g L?1 salinity showed significantly higher (P < 0.01) mean survival than those reared at 10 g L?1 salinity. The survival of larvae fed the bacterial‐based diet was higher compared with microalgal diet used in previous studies. The pPB had higher total polyunsaturated fatty acids and docosahexaenoic acid (DHA) than the microalgae, which had very high eicosapentaenoic acid (EPA). Larvae with very high ratios of DHA/EPA (>11) or/and ARA (arachidonic acid)/EPA (>5), attributable to their given diet, however suffered the highest mortality.  相似文献   

17.
Effect of isolipidic (62.7 ± 5.0 g kg?1) diets with protein levels of 204.6 (T20), 302.3 (T30), 424.6 (T40) or 511.0 g kg?1 (T50) on growth and survival in Nile tilapia (Oreochromis niloticus Linnaeus 1758) fry cultured for 70 days at one of four salinities (0, 15, 20 and 25 g L?1) was evaluated. A bifactorial (4 × 4) design was used with 16 treatments run in triplicate and 20 fry (0.25 ± 0.04 g) per replicate under semi‐controlled conditions. Four independent, recirculating systems (one per salinity level) were used, each one with 12 circular tanks (70 L capacity), filters and constant aeration. The different salinities had no significant effect on growth. Weight gain improved significantly as dietary protein content increased, although organisms fed the T50 diet had a lower growth rate. Survival was highest (98.33%) in the T50/15 (protein/salinity levels) treatment and lowest (71.0%) in the T20/20 treatment, with no pattern caused by the variables. The T40/25, T40/20 and T50/0 treatments produced the most efficient growth and feed utilization values while the T20 treatments at all the salinities resulted with the lowest performance. With the exception of the T50 treatments, a non‐significant tendency to increased weight gain was observed as water salinity increased, suggesting that the salinity of the culture environment does not influence dietary protein requirements in Nile tilapia O. niloticus fry.  相似文献   

18.
Abstract.— Tko experiments were conducted to determine the effects of salinity on growth and survival of mulloway Argyrosomus japonicus larvae and juveniles. First, 6-d-old larvae were stocked into different salinities (5, 12.5, 20, 27.5 and 35 ppt) for 14 d. Larvae grew at all salinities, but based on results for growth and survival, the optimum range of salinity for 6-d-old to 20-d-old larvae is 5–12.5 ppt. During this experiment larvae held in all experimental salinities were infested by a dinoflagellate ectoparasite, Amyloodinium sp. Degree of infestation was affected by salinity. There were very low infestation rates at 5 ppt (0.2 parasites/larva). Infestation increased with salinity to 20 ppt (33.1 parasites/larva), then declined with salinity to 35 ppt (1.5 parasites/larva). For the second experiment, juveniles (6.1 ± 0.1 g/fish) were stocked into different salinities (0.6, 5, 10, 20 and 35 ppt) for 28 d. Juveniles were removed from freshwater 3 d after transfer as they did not feed, several fish died and many fish had lost equilibrium. However, when transferred directly to 5 ppt. these stressed fish recovered and behaved normally. Trends in final mean weight and food conversion ratio of juvenile mulloway suggest that fish performed best at 5 ppt. Although salinity (5 to 35 ppt) had no significant ( P > 0.05) effect on growth, survival, or food conversion ratio of juveniles, statistical power of the experiment was low (0.22). Based on these results we recommend that mulloway larvae older than 6 d be cultured at 5 to 12.5 ppt. Optimum growth of juveniles may also be achieved at low salinities.  相似文献   

19.
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 (DOP) was lowest at 35 g L?1 and highest at 20 g L?1. Thus, the minimum DOP 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.  相似文献   

20.
The present study evaluated various sodium and potassium concentrations in hatchery water to determine which proportions would be optimal for Macrobrachium rosenbergii larviculture. Using a closed RAS system (60‐L), experiments were conducted in two stages. In the first stage, larval quality parameters were compared among triplicate treatments of sodium (2000, 3000, 4000 and 5000 mg L?1) and potassium (100, 150, 200 and 250 mg L?1). During the second stage, these same parameters were compared from interactions of the two best concentrations determined in the first stage. Initial larval density was fixed at 100 larvae L?1 and larval quality parameters such as larval stage index (LSI), larval condition index (LCI), larvae dry weight, survival (%), LC50‐24 h for formalin stress and time of the first postlarvae (PL) appearance were measured. Results showed that during the early larval period time LSI, LCI and survival parameters were affected only by potassium and the interaction with sodium was not significant. At a later period of the larval development, interactions between both sodium and potassium were measurable for LSI (P < 0.05) while the interactions on LCI and survival were not significant. Measurable differences among the combined treatments 4000 mg L?1 sodium and 150 mg L?1 potassium resulted in the best performance for M. rosenbergii larviculture. This concentration also provided the highest final survival to PL metamorphosis (40.6 ± 2.5%) which was at least 10% higher than the other treatments.  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号