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1.
  • 1.1. The acute toxicity of endosulfan was determined for the freshwater rotifer Brachionus calyciflorus.
  • 2.2. The mean 24 hr lc50 value for endosulfan was 5.15 ppm with a coefficient of variation of 14.7%.
  • 3.3. Rotifers were exposed at two sublethal concentrations (1.5–2.0 ppm) of endosulfan for bioaccumulation experiments, for an exposure time of 24, 48, 72 and 96 hr. The rotifers were fed with Nannochloris oculata (5 × 105cell/ml).
  • 4.4. The highest accumulation of endosulfan was found 24 hr after the start of the exposure to 1.5 ppm of the toxicant. A steady-state concentration in rotifer was reached between 24–48 hr, followed by a gradual decrease until 96 hr.
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2.
  • 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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3.
  • 1.1. Eel were exposed to a sublethal concentration of lindane (0.335 ppm) for 6, 12, 24, 48, 72 and 96 hr.
  • 2.2. Concentrations of glycogen, glucose, lactate, pyruvate and lipids were determined in gill tissue after lindane exposure.
  • 3.3. Gill glycogen descreased and glucose levels increased at 6 hr of treatment, lactate and pyruvate concentration increased between 6 and 48 hr. Total lipid values decreased between 6 and 24 hr; thereafter, the levels increased up to 72 hr of exposure.
  • 4.4. Clear changes were found in all parameters tested in gill tissues. The observed effects of lindane on metabolism in fish are discussed in relation to acute stress syndrome.
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4.
  • 1.1. When Mytilus galloprovincialis were transferred from 38 to 19%. sea water (S), the metabolism became anaerobic for at least 8 hr. After 24 hr the animals were entirely aerobic again.
  • 2.2. Upon transfer to 19%. S, the total free amino acid concentration in haemolymph doubled within 4 hr, remaining nearly constant thereafter, up to 48 hr.
  • 3.3. In the posterior adductor muscle a strong decrease of alanine and glycine occurred at 48 hr exposure to 19%. S, and a smaller decrease of glutamate; taurine remained relatively constant. When transferred again to 38%. S after 14 days, a strong overcompensation occurred in the concentrations of alanine and proline, and a smaller overcompensation in those of threonine and serine.
  • 4.4. In the gill no distinct change in the amino acid pool occurred during 14 days of exposure, with the exception of a decrease in serine. When transferred again to 38%. S, a strong overcompensation occurred in alanine, proline, glycine and serine, and a smaller in glutamate and threonine.
  • 5.5. No evidence for anaerobic metabolism in the decrease of the amino acid pool was found.
  • 6.6. M. galloprovincialis is less able to adapt to low salinities than the more euryhaline M. edulis.
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5.
  • 1.1. Aroclor 1254 had an influence on biochemical composition of phytoplankton Phaeodactylum tricornutum.
  • 2.2. Total lipid content of Arocolor 1254 treated phytoplankton ranged from 90 to 40%, total carbohydrates from 5 to 50%, while protein content was almost unchanged.
  • 3.3. The observed rapid and significant increase in lipid content (150%) within the first 24 hr could be ascribed to their protective role.
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6.
  • 1.1. Effects of hypoxia were investigated in red abalones (Haliotis rufescens) using a flow-through exposure system and in vivo31P NMR spectroscopy.
  • 2.2. Following seawater acclimation, abalones were exposed to air for 1 hr, then seawater for 2.5 hr to check recovery; parallel controls were performed without air exposure.
  • 3.3. In foot muscle, hypoxia produced a decrease in phosphoarginine concentration and intracellular pH, an increase in inorganic monophosphate concentration, and no change in that of ATP; upon resubmergence, all effects generally recovered.
  • 4.4. The changes induced by hypoxia during normal tidal changes are consistent with the blockage of mitochondrial oxidative phosphorylation.
  • 5.5. Use of in vivo NMR allows measurement of the biochemical effects of natural stress factors in live, intact aquatic organisms in the laboratory.
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7.
  • 1.1. The phenoloxidase activity, protein and carbohydrate levels were studied for 24 hr in the hemolymph of the migratory grasshopper, Melanoplus sanguinipes after artificial wounding of the insect cuticle or the injection of Beauveria bassiana conidia.
  • 2.2. Injection or wounding induced a primary response and phenoloxidase activity was found to increase within 10–60 min. The values for phenoloxidase activity in viable B. bassiana-injected insects exhibited a secondary response, i.e., an increase 24 hr after injection.
  • 3.3. In wounded insects and those injected with inactivated conidia, the phenoloxidase activity receded after the initial increase and remained at low levels.
  • 4.4. Protein concentrations in the hemolymph increased immediately after infection and wounding and returned to basal levels during the course of the experiment.
  • 5.5. Injection of viable B. bassiana resulted in a gradual increase in the protein concentrations between 12 and 24 hr.
  • 6.6. There was no apparent change in the carbohydrate levels in either B. bassiana-infected or wounded insects.
  • 7.7. These results are discussed in relation to their possible role(s) and interrelationships in the immune response to infection or wounding. Furthermore, we suggest that a “factor” is released after mechanical injury of the integument.
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8.
  • 1.1. Cells of tentacles and body wall of the sea anemone Condylactis gigantea behaved as simple osmometers during 5hr exposure to 50, 67, 83, 100 and 125% sea-water.
  • 2.2. All intracellular water appeared to be osmotically active.
  • 3.3. Cell sodium, chloride and total osmolyte content remained invariable, with taurine decreasing and potassium increasing as sea-water concentration was reduced.
  • 4.4. Tissues, as a whole, exhibited a pseudoregulatory response to changes in salinity as the large and osmotically inert extracellular space buffered volume changes to a considerable extent.
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9.
  • 1.1. Inorganic phosphate (Pi) was absorbed rapidly by suspension-cultured cells of Catharanthus roseus which had previously been cultured in Pi-free Murashige Skoog medium.
  • 2.2. The intracellular levels of ATP, ADP and 5-phosphoribosyl-l-pyrophosphate (PRPP) increased markedly during the 24 hr which followed the addition of Pi (1.25mM).
  • 3.3. Availability of PRPP in vivo, estimated by the measurement of nucleotide synthesis from [8-14C]adenine, was also increased by addition of Pi.
  • 4.4. Only a 20% increase in the maximum catalytic activity of PRPP synthetase was observed in extracts of cells, prepared 24 hr after addition of Pi.
  • 5.5. In contrast to results for mammalian PRPP synthetase, the activity of PRPP synthetase, partially purified from Catharanthus roseus, was inhibited by concentration of Pi greater than 5mM.
  • 6.6. The mechanisms involved in the increased availability of PRPP and the synthesis of adenine nucleotides in the plant cells cultured in Pi-containing medium are discussed.
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10.
  • 1.1. Lipid, glucose and glycogen concentrations were measured in different tissues of the crab Chasmagnathus granulata during emersion.
  • 2.2. After 6 hr of emersion no reduction in the total amount of carbohydrates was found to occur, suggesting that a general metabolic arrest was taking place.
  • 3.3. A transitory increase in haemolymphatic glucose and lipid levels was observed. Possible causes are therefore discussed in relation to changes in the flux of substrates for energy production.
  • 4.4. The mobilization of carbohydrates and lipids to the gills, observed only during summer, may be concerned with energy supplying for ionic regulation.
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11.
  • 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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12.
  • 1.1. P. elarki is an oxyconformer, with an oxygen uptake rate of 144 ± 4 μl/g wet wt/hr at oxygen tensions above 90% saturation and an uptake rate of 18 ± 3 μl g wet wt/hr at 15 torr.
  • 2.2. Between 159 and 40 tort, blood pH decreases slightly from 7.77 ± 0.03 to 7.65 ± .04, and at 15 torr, blood pH drops to 7.36 ± 0.06.
  • 3.3. At normoxia, blood lactate levels are low at 0.66 ± 0.01 mM/l blood. After 2 and 5 hr exposure to 15 tort, blood lactate levels increase to 3.29 ± 0.47 and 8.91 ± 0.14 mM/l blood, respectively. Upon return to normoxia, blood lactate levels decrease and are comparable to normoxic controls after 13 hr.
  • 4.4. During mild hypoxia, P. elarki maintains adequate oxygen transport by utilizing a high O2 affinity hemocyanin in conjunction with a low metabolic demand by its tissues.
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13.
  • 1.1. Effect of controlled up- and down-shifts of growth temperature on the antioxidant enzymes activities and lipid peroxidation were investigated in intact cells of Cyanobacterium synechocystis PCC 6803 acclimated at different growth temperature.
  • 2.2. Algal cells grown at 36°C were treated at 20 and 43°C as down- and upward-shifts of growth temperature for 24 hr, respectively. At the down-shift of growth temperature the superoxide dismutase, catalase and glutathione peroxidase were significantly increased with concomitant decrease in protein content.
  • 3.3. These parameters showed similar temperature dependencies in the up-shift of growth temperature, they were decreased significantly.
  • 4.4. The increased hydroxyl (HO) radical and malonyldialdehyde (MDA) formation, when algal cells exposed to down-shift of growth temperature, supposedly due to stimulated production of superoxide radicals (O2) and hydrogen peroxide (H2O2) at lower temperature.
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14.
  • 1.1. Studies characterizing glucose transport in the frog sartorius were performed.
  • 2.2. For nonstimulated and stimulated muscles, intracellular 2-deoxyglucose exceeded 2-deoxyglucose-6-phosphate at 15 min, showed little further increase, and was maintained below the extracellular concentration for 2 hr.
  • 3.3. Accumulated 2-deoxyglucose-6-phosphate did not inhibit glucose transport.
  • 4.4. Unlike in adipocytes, basal and stimulated 2-deoxyglucose transport showed no difference in sensitivity to N-carbobenzoxy-glycyl-l-phenylalaninamide.
  • 5.5. Phenylarsine oxide blocked contraction-enhanced 2-deoxyglucose uptake.
  • 6.6. These results suggest that the glucose transporter of the sartorius exhibits auto-regulation, and that basal transport is not regulated by the same process as in adipocytes.
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15.
  • 1.1. To evaluate changes in high-energy phosphate metabolism in the water scorpion (Ranatra chinensis) under restraint and cold water-warm water stresses, in vivo [31P]NMR spectra were obtained.
  • 2.2. Under restraint stress, arginine phosphate (Arg-P) decreased by 10% after 1 hr and remained at that level thereafter, while β-ATP showed negligible changes over 6 hr.
  • 3.3. As the water temperature gradually increased or decreased, the relative concentration of Arg-P decreased due to enzyme regulation.
  • 4.4. Repeated cold water-warm water stress, which consisted of repeated 15 min exposures to cold water (5°C) followed by 15 min exposures to warm water (30°C) caused distinct decreases in Arg-P and β-ATP concentration. These decreases were dependent on the frequency of exposure.
  • 5.5. Phosphomonoesters (PME) increased not only with restraint stress but also with cold water-warm water stress.
  • 6.6. The effect of cold water-warm water stress on high-energy phosphate metabolism was greater than that of restraint stress.
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16.
  • 1.1. Embryonic and posthatch turkey skeletal muscle development was compared in in vitro studies using clonal-derived embryonic myoblasts and satellite cells.
  • 2.2. Although population doubling times were similar between the two lines (25.4 hr for satellite cells and 26.4 hr for embryonic myoblasts), embryonic myoblasts consistently began log phase growth 24 hr earlier than satellite cells.
  • 3.3. Differentiation (fusion) of embryonic myoblasts was maximized by 36 hr in Dulbecco's Modified Eagle's Medium containing 1% horse serum compared with 72 hr for satellite cells.
  • 4.4. When administered a serum-free medium which supports proliferation of turkey satellite cells, embryonic myoblasts differentiated to form myotubes.
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17.
  • 1.1. Daphnia magna were exposed for 24 hr to 14C-labelled pentachlorophenol (PCP) at an initial concentration of 20μg/l in the incubation water. Occurrence of free PCP and its metabolites were measured both from the animals and the water.
  • 2.2. Hydrophilic metabolites excreted into water were analysed, after acid or enzymatic hydrolyses, with a liquid-liquid extraction and TLC.
  • 3.3. PCP was metabolized and excreted, perhaps solely, via the sulphate conjugation. The average excretion rate, 2.65nmol/g/hr, accounted for 35% of the absorption rate measured at the start of exposure.
  • 4.4. Neonate daphnids had an equal ability to metabolize PCP as the older animals. Bioconcentration in young animals was, however, only 23% of that in adult ones.
  • 5.5. Effect of naturally humic water on metabolization and excretion of PCP was negligible.
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18.
  • 1.1. A comparison of proteolytic and protease inhibitory activity, and ecdysteroid levels in body fluids was made between normal larvae of the flesh fly, Sarcophaga bullata, and those that had been water-stressed for two days.
  • 2.2. The course of proteolytic activity in water stressed flies decreases 6 hr after beginning the experiment and remains low in comparison with control flies.
  • 3.3. The course of protease inhibitors exhibits a mirror image pattern to proteases.
  • 4.4. Ecdysteroid pattern shows two peaks in control animals: minor at 24 hr and major at pupariation, in experimental animals: at 1 hr, at 6 hr and at white pupal stage.
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19.
  • 1.1. The histopathology of zebra mussel populations (Dreissena polymorpha) which were transplanted and exposed in baskets in the Dutch sector of the River Maas (5 locations) were compared with indigenous wild mussels at the same locations and at a clean reference site in the Ijsselmeer.
  • 2.2. All groups were sectioned histologically and examined to quantify cytological damage and pathology of a wide range of tissues, as well as to examine parasitology and to assess their reproductive state.
  • 3.3. Results show a significant reduction in general cytological quality and an increase in observed pathological conditions in the wild populations at the 3 downstream stations.
  • 4.4. The transplanted (active biomonitoring) groups of mussels clearly showed a similar trend in condition after only 42 days exposure at these sites.
  • 5.5. The influence of an industrial spillage of Cd in the Maas during the exposures is examined against this background of locally varying “health”.
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20.
  • 1.1. Reducing conditions must be maintained throughout the procedure of isolating metallothioneins from crabs. Dithiothreitol is preferred to 2-mercaptoethanol for long-term protection.
  • 2.2. Two metallothioneins (10,100 and 4100 mol. wt, respectively) in the hepatopancreas of the crab Carcinus maenas showed great variability between individual crabs as to their presence and to their contents of Zn, Cu and Cd.
  • 3.3. The 10,100 mol. wt metallothionein was induced in the laboratory by exposure to Cu and Cd, and variably by Zn-exposure. Laboratory induction did not raise significantly the total metal content of 0.88 ± 1.13 g atoms/mol protein of this metallothionein in crabs from the Firth of Clyde, Scotland.
  • 4.4. The 4100 mol. wt metallothionein was not induced in the laboratory by exposure to Cu, Cd or Zn. This metallothionein in crabs from the Firth of Clyde, Scotland, contained 0.27 ± 0.34 g atoms of total Cu, Cd and Zn per mole of protein.
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