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1.
  • 1.1. The oxygen consumption of the marine teleost, Lichia amia was investigated under controlled laboratory conditions.
  • 2.2. The routine oxygen consumption showed a strong circadian rhythm with the fish being mainly active during the light period.
  • 3.3. The specific mass exponent (dimension: μg O2/g/hr) is temperature independent and ranges from 0.27–0.29.
  • 4.4. Starving the fish results in a mean decrease in active, routine and standard oxygen consumption of 21%, 24% and 20%, respectively.
  • 5.5. Feecling led to an increase in the oxygen consumption of the teleosts, with the mean metabolic rate over the 24 hr that followed, being 58% and 50% higher for fish that had been starved for 162hr and 40 hr, respectively.
  • 6.6. Apparent SDA showed some variation and ranged from 6.0 to 35.5%.
  • 7.7. The results obtained are generally in agreement with those recorded for other teleosts.
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2.
Analyses by mass spectrometry of carbon/oxygen isotope compositions of lapilli and sagittal otoliths in the catadromous New Zealand mullet Mugil cephalus permit us to draw the following conclusions:
  • 1.1. Information on the type of aquatic environment a larval fish has experienced can be obtained from otoliths of the adult in two ways: drilled cores along the long axis of the sagitta can be analysed sequentially for carbon/oxygen isotope composition.
  • 2.2. The oldest isotope ratios, representing the time when the first aragonite was laid down, are closest to the centre, while material nearer to the edges of the earstone reflects carbon/oxygen isotope values of the environment the fish had experienced at the time of capture.
  • 3.3. The second approach involves the lapilli. These otoliths are universally smaller than the sagittae in adult fish, but at hatching the two are of equal size in many species of fish, including the mullet.
  • 4.4. Consequently, the lapillus carbon/oxygen isotope ratio closely resembles that of the larval environment (in our case, the estuarine waters of New Zealand's North Island), whereas averaged carbon/oxygen isotope ratios of the sagittae more closely agree with those of river water.
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3.
  • 1.1. The rate of oxygen consumption has been monitored continuously in M. edulis during acute exposure to high sublethal concentrations of formaldehyde, phenol and benzene and subsequent recovery periods of 96 hr.
  • 2.2. The results are discussed in relation to changes in the electrochemical potential difference of sodium, the content of ATP and the tissue concentration of strombine.
  • 3.3. After exposure to benzene and phenol, an increase in the rate of oxygen consumption that could not be explained by oxygen debt from the exposure period was observed.
  • 4.4. Depression of the rate of oxygen consumption after exposure to formaldehyde may be explained by a reduced ability to extract oxygen from the water.
  • 5.5. The pattern of oxygen consumption and behavioural responses, as well as the combined changes in the biochemical markers, were distinctly different in the three cases.
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4.
  • 1.1. The ventilatory mechanism, gill area, sites of oxygen uptake, oxygen consumption and activity of a crab from south Brazil, Chasmagnathus granulata, were investigated.
  • 2.2. The oxygen uptake seems to be restricted to the gill lamellae.
  • 3.3. The gill area varies with the wet body weight, being relatively higher in smaller animals. There is not a significative reduction of the gill area in relation to species of the infralittoral zone.
  • 4.4. C. granulata presents a mechanism for recirculating the water of its branchial chamber when exposed to atmospheric air.
  • 5.5. The oxygen consumption and activity are reduced when the animals are exposed to atmospheric air. The reduction in the oxygen consumption may be related to the poorly adapted respiratory system, while the decrease in activity may be a mechanism for saving energy during this hypoxic period.
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5.
  • 1.1. The Root effect was evaluated in hemolysates from 26 species of bony fish and 20 species of cartilaginous fish found on the Brazilian southeastern coast.
  • 2.2. Teleost Root shifts, with a single exception, are correlated with the presence of the choroid rete mirabile but not with its counterpart in the swimbladder.
  • 3.3. Five ray species displayed weak and moderate Root effects despite the absence of choroid and swimbladder rete.
  • 4.4. The presence and intensity of the Root effect is probably primarily related to the high oxygen demand of the retina and with the importance of visual perception in fish.
  • 5.5. In marine teleosts the magnitude of the Root effect seems to be associated with the presence and size of both the choroid rete and the pseudobranch.
  • 6.6. An antioxidant protection of the fish eyes can be advocated for the pseudobranch.
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6.
  • 1.1. The nonfaecal nitrogenous excretion rate in starved sterlet fingerlings and fingerlings fed on different rations was investigated. The weight of the fish and temperature of the water was 43 g and 17.5°C, respectively.
  • 2.2. In the nonfaecal excrements of starved sterlets the ammonia: urea ratio was substantially lower than in teleosts. This ratio was found to be 1.4:1.
  • 3.3. In fed sterlets the urea excretion rate was higher than in starved ones but independent of ration size.
  • 4.4. During the day the urea excretion rate in sterlets was constant.
  • 5.5. The ammonia excretion rate accelerated 2 hr after feeding and reached its peak duration 6–11 hr after depending on the ration size.
  • 6.6. Total ammonia output in the sterlet increased following the increase of ration size up to 8.4% of body wt. Further increases in ration size did not cause the corresponding elevation of ammonia excretion rate.
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7.
  • 1.1. The effects of Triton X-100 treatment on the lipid contents and functional properties of hake myofibrils from pre- and post-spawned fish were investigated.
  • 2.2. Differences in lipids, biochemical and functional properties of hake myofibrils related to the gonadal condition of fish were observed.
  • 3.3. Triton X-100 treatment removed 65% of polar lipids in myofibrils from pre-spawned fish and only 10% in myofibrils from post-spawned fish.
  • 4.4. Triton X-100 increased the Hill coefficient to 1.5 in an allosteric type of reaction for the myofibrillar Mg2+-ATPase from pre-spawned hake.
  • 5.5. The detergent effect observed on the contraction response was greater in myofibrils from prespawned fish than in post-spawned fish.
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8.
  • 1.1. Measurements of the rate of nitrogen consumption, total nitrogen and ammonia excretion and nitrogen absorption of bream, Abramis brama L. (body weight range 0.4–519 g wet wt) were made at 10, 15 and 20 C.
  • 2.2. Fish were fed once daily on live zooplankton collected in Lake Balaton and cultured Tubifex sp. at 5–15% of their body weight.
  • 3.3. Fish size and temperature had a combined effect on the rate of total nitrogen excretion. Total nitrogen excretion did not increase proportionally with an increase in consumption.
  • 4.4. On average, 52–80% of the nitrogen consumed with food was excreted by bream.
  • 5.5. The greatest part of total nitrogen excretion was ammonia and its proportion in the total ranged between 53 and 75%.
  • 6.6. Temperature did not have any significant effect on the proportion of excreted ammonia and the rate of excreted total nitrogen was the only factor determining its proportion in the total.
  • 7.7. The rate of nitrogen absorption of bream was surprisingly very high.
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9.
  • 1.1. The actions of piroxicam, a nonsteroidal and noncarboxylic anti-inflammatory drug, on the metabolism of the isolated perfused rat liver were investigated. The main purpose was to verify if piroxicam is also active on glycogenolysis and energy metabolism, as demonstrated for several carboxylic nonsteroidal anti-inflammatories.
  • 2.2. Piroxicam increased oxygen consumption in livers from both fed and fasted rats.
  • 3.3. Piroxicam increased glucose release and glycolysis from endogenous glycogen (glycogenolysis).
  • 4.4. Gluconeogenesis from lactate plus pyruvate was inhibited.
  • 5.5. The action of piroxicam on oxygen consumption was blocked by antimycin A, but not by atractyloside.
  • 6.6. The action of piroxicam in the perfused rat liver metabolism seems to be a consequence of its action on mitochondria.
  • 7.7. It can be concluded that inhibition of energy metabolism and stimulation of glycogenolysis are not specific properties of carboxylic nonsteroidal anti-inflammatory drugs.
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10.
  • 1.1. Indian River male broiler chickens growing from 7 to 28 days of age were fed diets containing 12, 18, 24 and 30% protein + 0 or 1 mg triiodothyronine (T3)/kg of diet to study energetic costs of lipogenesis and the use of various substrates for in vitro lipogenesis.
  • 2.2. De novo lipid and CO2 production were determined in the presence of [1-14C]pyruvate, [2-14q]pyruvate, [3-14C]pyruvate, [2-14C]acetate and [U-14C]alanine.
  • 3.3. Oxygen consumption was determined in mitochondrial preparations to estimate the energetic costs in expiants synthesizing lipid.
  • 4.4. Radiolabeled CO2 derived from [1-14C]pyruvate was used as an estimate of coenzyme A availability in liver expiants. Lipids derived from [2-14C]pyruvate, [2-14C]acetate and [U-14C]alanine estimate relative substrate efficiency.
  • 5.5. Labeled CO2 production from [1-14C]pyruvate was greatest in that group fed a 12% protein diet and least in the group fed a 30% protein diet.
  • 6.6. In addition, T3 increased CO2 production from [1-14C]pyruvate.
  • 7.7. The production of 14CO2 from the second carbon of pyruvate or acetate was increased by T3.
  • 8.8. The low-protein diet (12% protein) increased (P <0.05) lipogenesis.
  • 9.9. Adding T3 to the diets decreased carbon flux into lipid from all substrates, but increased CO2 production from all substrates without changing stage 3 and 4 respiration rates in mitochondrial preparations.
  • 10.10. These observations imply that coenzyme A availability may have regulated de novo lipogenesis in the present study.
  • 11.11. It was also concluded that previously noted effects of T3 on intermediary metabolism may involve metabolic pathways that do not involve changes in mitochondrial function.
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11.
  • 1.1. We investigated the effects of the ingestion of naturally occurring glucosinolates in rapeseed meal on growth rate, metabolic efficiency and respiratory rate in larvae of the yellow mealworm, Tenebrio molitor L.
  • 2.2. In our feeding studies, larvae were reared on one of seven different diets, including a whole ground wheat control diet and rapeseed meal from six rapeseed varieties. Dry weight gain of larvae and dry food assimilated were measured after 4 weeks of rearing, and the conversion of food into insect biomass was determined. The results may be explained by variations in the glucosinolates content of the diets.
  • 3.3. The effect of glucosinolates on food consumption, larval growth, expired carbon dioxide, oxygen uptake and respiratory quotient were studied.
  • 4.4. Glucosinolates did not reduce food assimilation or growth after 1 day of experimentation, but they caused some inhibition of respiratory exchanges and increased the RQ ratio.
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12.
  • 1.1. The urate, urea and ammonia content of the whole egg of the Japanese quail was measured in late incubation in eggs subject to different rates of water loss.
  • 2.2. High rates of water loss substantially increased egg urate content, but had little or no effect on urea or ammonia content.
  • 3.3. Allopurinol, an inhibitor of urate synthesis, reduced egg urate content to low levels, but produced no effect on urea content, and a small reduction in ammonia content.
  • 4.4. The urea concentration of the embryo was lower than in allantoic fluid.
  • 5.5. It is concluded that urate production by the avian embryo is primarily concerned with the modification of allantoic fluid composition.
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13.
  • 1.1. Preparative Isoelectric focusing (PIEF) was used to isolate hydroxylasic and dehydrogenasic activities, at different pI.
  • 2.2. The fraction at pI 4.7 and 4.9 displays a pure dehydrogenase activity (substrate l-DOPA).
  • 3.3. This fraction did not react with tyrosine, either in the spot-test or in absorption spectra (200–620 nm), and did not exhibit any oxygen consumption.
  • 4.4. The fraction at pI 4.1 and 4.3 reacted with both l-DOPA and tyrosine as substrate, showing dehydrogenase and hydroxylase activity.
  • 5.5. The latter activity was confirmed by the oxygen consumption test, showing that molecular oxygen is used to ortho-hydroxylate tyrosine.
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14.
  • 1.1. Body temperature, oxygen consumption, CO2 production and muscle protein degradation rate were measured in the three quail lines selected for body size, a random bred line (RR) and two lines selected for large (LL) or small (SS) body size.
  • 2.2. The body temperature at 15 weeks of age was highest for small body size line and lowest for large body size line.
  • 3.3. The body temperature, oxygen consumption and CO2 production of females were significantly higher than that of males.
  • 4.4. The fractional degradation rate of muscle protein of SS, RR and LL lines were measured as 2.4, 1.6 and 1.2% per day in male, and 2.6, 1.7 and 1.4% per day in female.
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15.
  • 1.1. The effects of storage temperature (2, −20 and −80°C) and duration (3, 9 and 27 days) on plasma metabolites concentrations of lake trout fed three dietary protein levels (20, 40 and 60%) and a single lipid level (20%) for 28 days were investigated.
  • 2.2. Significantly high plasma urea and glucose concentrations were associated with low (20%) and high (60%) dietary protein intake in fish; while, high plasma creatinine concentration seems to characterize insufficient dietary protein and energy consumption.
  • 3.3. Deproteinization of plasma with 5.0% sulfosalicylic acid did not confer better storage stability for any of the plasma metabolites except ammonia which was significantly high in non-deproteinized samples when stored at 2°C over 3, 9 and 27 day periods.
  • 4.4. These studies suggest that non-deproteinized fish plasma can be stored at − 20°C without affecting the baseline concentrations of ammonia, creatinine and glucose for up to 9 days and, urea and total protein for up to 27 days.
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16.
  • 1.1. The oxygen consumption of red and green Carcinus in normoxic and hypoxic sea water was determined, using an oxygen electrode in a sealed respirometer.
  • 2.2. The red crabs had significantly higher “excited” oxygen uptake rates and a lower ability to compensate for hypoxia than the green crabs.
  • 3.3. Red Carcinus display an emersion response to declining oxygen at lower oxygen tensions than the green crabs.
  • 4.4. Mortality of red crabs exposed to prolonged anoxia was much greater.
  • 5.5. The relationship of these findings to the zonation of the two colour forms on the shore is discussed.
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17.
  • 1.1. Ependymins are unique, highly divergent secretory proteins of the fish endomeninx. Thus far, no homologous sequences have been characterized in mammals.
  • 2.2. Soluble ependymins are the predominant constituents of the cerebrospinal fluid of many teleost fish. A bound form of these glycoproteins is associated with the extracellular matrix probably with collagen fibrils. The latter may be the functional form of ependymins.
  • 3.3. Ependymins bind Ca2+ via N-linked sialic acid residues leading to a conformational transition.
  • 4.4. The molecular function of ependymins seems to be related to cell contact phenomena involving the extracellular matrix. For example, adhesive or anti-adhesive interactions may possibly influence ingrowing axons.
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18.
  • 1.1. The oxygen consumption of crabs in normoxic and hypoxic (50% O2) seawater was measured directly after collection.
  • 2.2. The influences of size and lunar cycles were removed by scaling the data.
  • 3.3. Strong negative correlations between low individual levels of O2 consumption and the ability to compensate for hypoxia were apparent in Wicklow (subtidal) crabs.
  • 4.4. Compensation for hypoxia was much greater on the flood tide than on the ebb.
  • 5.5. Crabs from Roscoff (intertidal) had lower levels of compensation than those from Wicklow.
  • 6.6. Size, sex and condition had no apparent effect upon these relationships.
  • 7.7. Crabs acclimated to laboratory conditions have not shown this tidal variation in compensation for hypoxia.
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19.
  • 1.1. Oxygen uptake attributable to Specific Dynamic Action (SDA) was measured in common carp, Cyprinus carpio L. (63.6–84.0 g) fed on 20, 35 and 50% dietary protein at 0.40 to 1.00% ration levels at 28°C.
  • 2.2. After feeding both SDA magnitude and mean peak oxygen consumption increased directly with dietary protein and ration levels. SDA duration was not significantly related to dietary protein but significantly increased with ration levels.
  • 3.3. SDA coefficients were 8.99, 13.51 and 15.94% with 20, 35 and 50% dietary protein showing a direction relationship to the protein content. The SDA coefficient did not change with ration size.
  • 4.4. SDA models resulting from this work are of great interest for the aquaculturist, as post-feeding oxygen requirements in an intensive fish culture can be predicted where dietary protein and ration levels are known.
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20.
  • 1.1. Adenosine 5'-phosphoramidate hydrolase of 29 kDa was isolated from rat liver cytosol.
  • 2.2. It consisted of two subunits of 14 kDa.
  • 3.3. It hydrolyzed nucleoside 5'-monophosphoramidates into nucleoside 5'-monophosphates and ammonia, while it did not hydrolyze adenylyl phosphoramidate, adenylyl imidodiphosphate and N-phosphorylated compounds like phosphocreatine, Nω-phosphoarginine, 6-phospholysine and 3-phosphohistidine.
  • 4.4. Divalent cations and cyclic AMP had no effect on the hydrolytic activity.
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