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1.
  • 1.1. The relationship between nitrogen metabolism and osmoregulation has been studied in the prawn Palaemon elegans (Rathke) following sudden exposure to hyper- and hyposaline conditions.
  • 2.2. Animals acclimated to a salinity of 30‰ showed a pronounced increase in the rates of ammonia excretion during the first 2 hr after transfer to lower salinities. These gradually declined during the next 6 hr to rates that were significantly higher than that of control animals (30‰) and were maintained throughout the rest of the experiment.
  • 3.3. Rates of ammonia excretion in animals transferred to hypersaline conditions (40‰) fluctuated considerably during the experiment. It was consistently observed, however, that there were two periods during the experiments when ammonia excretion rates had negative values indicating that NH+4 ions were being taken up by the prawns.
  • 4.4. Experiments in which small quantities of (NH4)2SO4 containing the stable isotope 15N were added to the sea-water confirmed that P. elegans was able to take NH+4 ions from the sea-water.
  • 5.5. Changes in the Na+ ion concentration in the blood and the changes in free amino acid concentration in the blood and in the muscle after exposure to differing salinities were also determined. Their significance and relationship to the observed changes in the rates of ammonia excretion are discussed.
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2.
  • 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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3.
  • 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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4.
  • 1.1. Oxygen consumption and production rates were measured in two species of colonial ascidians that contained the algal symbiont, Prochloron.
  • 2.2. Despite differences in size and habitats, the colonies showed similar rates of oxygen consumption and production.
  • 3.3. Oxygen production by the colonies was light dependent.
  • 4.4. Based on the data presented, the symbiosis is similar to other algal-invertebrate symbioses in producing more oxygen than is consumed when illuminated.
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5.
  • 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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6.
  • 1.1. Oxygen uptake and grazing rates of juvenile bivalve molluscs Mytilus edulis, Mya arenaria, Geukensia demissa, Placopecten magellanicus and Crassostrea virginica were measured following 1 hr exposure to bloom concentrations (106 cells/1) of the toxic dinoflagellate Alexandrium tamarense (GT429) using a non-toxic clone of the same species (PLY 173) as control.
  • 2.2. For all bivalves, prefeeding estimates of V̇O2 were similar to postfeeding values and values recorded 24 hr after exposure to bloom conditions.
  • 3.3. V̇O2 was similar for bivalves fed on both the toxic and non-toxic strains of A. tamarense suggesting that there were no adverse effects on V̇O2 following 1 hr exposure to toxic GT429.
  • 4.4. Bivalves differed in their rates of grazing between toxic GT429 and non-toxic PLY 173. Similar grazing rates were recorded for M. edulis and G. demissa. For P. magellanicus and M. arenaria reduced rates of clearance were recorded in GT429 compared with the non-toxic strain.
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7.
  • 1.1. In sea-water, adult salmon (S. salar) exchange an average of 12.6% of total body sodium/hr.
  • 2.2. Following transfer to fresh water sodium uptake follows Michaelis-Menton kinetics. Fmax = 2.40 mmol Na/1 ECF/hr, Km = 0.26 mmol Na/1. The uptake system is fully activated immediately following transfer to fresh water.
  • 3.3. Post smolts adapted to sea-water for 3 months take up sodium at only one third of the rate of adult fish following return to fresh water.
  • 4.4. The concentration of prolactin in the plasma is low in sea-water adapted fish and does not rise during the first 8 hr in fresh water.
  • 5.5. At pH 5 sodium uptake is reduced by almost 90%, even in the absence of aluminium, but recovers immediately on return to neutral water.
  • 6.6. At pH 5 and 20 μmol Al/1 there is little further effect on sodium uptake but after 6 hr in aluminium the inhibition of sodium uptake continues after return to neutral aluminium fresh water and uptake is only 50% of normal 24 hr later.
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8.
  • 1.1. The concentrations (mM) of osmolytes in the coelomic fluid of Luidia clathrata kept at 25‰S seawater (control individuals) were: 345, Na+; 10, K+; 10, Ca2+; 44, Mg2+; 387, Cl; 0.67, amino acids; 0.09, NH4+.
  • 2.2. When individuals were transferred from 25‰S to 15‰S or 35‰S, the concentrations of inorganic ions in the coelomic fluid usually equilibrated within 24hr and became the same as those in the medium.
  • 3.3. The intracellular water content (g intracellular H2O/g solute-free dry tissue) of the pyloric caeca and tube feet of control individuals throughout the experiment was 2.13 and 5.40, respectively.
  • 4.4. In tissues of individuals transferred to 15‰S, the intracellular water content increased by an average 50% in 12 hr but returned to 19% above control levels during 1 week.
  • 5.5. In tissues of individuals transferred to 35‰S, the intracellular water content decreased by an average 17% in 12 hr and did not change during 1 week.
  • 6.6. Luidia clathrata is an osmoconformer and partial cell volume regulator within the seasonal salinity range it encounters.
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9.
  • 1.1. The oxygen consumption by P. californiensis postlarvae (mean wt = 0.38 g) was determined at five different temperatures and four salinities.
  • 2.2. The O2 in each chamber was recorded at 10 min intervals for 1 hr. The time course of oxygen depletion was independent of O2 concentration down to 1.6 mg/l.
  • 3.3. Oxygen consumption increased with temperature from 0.0045 mg/g/min at 19°C, to 0.0142 mg/g/min at 35°C. The thermal coefficient (Q10) indicated a very high sensitivity of the postlarvae to temperature variations at 19–23°C.
  • 4.4. The results show that oxygen consumption significantly depends on temperature (P < 0.001) while salinity has only a marginal effect.
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10.
  • 1.1. The modulation of lipid dynamics and lipid protein interactions were studied in rat brain synaptosomal plasma membranes (SPM) up to 24 hr after exposure to cadmium (Cd).
  • 2.2. The activity of acetylcholinesterase and adenylate cyclase showed a considerable decrease after 6 hr of Cd exposure, followed by a progressive increase up to 24 hr.
  • 3.3. SPM chemiluminescence showed a maximum decrease at 12 hr, demonstrating a considerable increase in lipid peroxidation.
  • 4.4. SPM of Cd-exposed animals showed a statistical significant increase in fluorescence anisotropy parameter [(r0/r) — 1]−1 at 18 and 24 hr compared to SPM of the control, indicating a decrease of membrane fluidity.
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11.
  • 1.1. Short-chain fatty acid concentration was 180mmol/l in the proximal colon and decreased to 108 mmol/l in the rectum.
  • 2.2. Fermentation in chymus from different regions of the colon, showed the pattern of end products to reflect the substrate and not the site of the colon.
  • 3.3. Isolated mucosa from proximal and distal colon had electroneutral sodium absorption of 4.8 ± 0.2 and 2.9 ± 0.8 μeq/cm2 hr in bicarbonate free media, which was abolished in the absence of chloride.
  • 4.4. Electroneutral sodium absorption was enhanced by short-chain fatty acids in the proximal colon and could be described by Michaelis-Menten kinetics with Km 2.0–11 mmol/l and Jm 1.6–3.6μeq/cm2 hr. In the distal colon the stimulation was smaller and propionate even inhibited sodium absorption.
  • 5.5. Butyrate was absorbed in the proximal colon, whereas acetate and propionate, and butyrate in the distal colon had a flux ratio of one.
  • 6.6. Amiloride (5 mmol/l) inhibited sodium absorption and net butyrate absorption.
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12.
  • 1.1. Fundamental chitin digestion characteristics of Crassostrea virginica crystalline style were investigated.
  • 2.2. Optimum temperature and pH were 34°C and 4.8. respectively.
  • 3.3. The colloidal regenerated chitin (0.56mol/0.5 ml: GlcNAc equivalents) was saturating under all enzyme levels encountered.
  • 4.4. There was no evidence of end product inhibition, even after 100 hr incubation.
  • 5.5. Calculated Km for the chitinase complex was 1.19mM when determined using a 30 min assay, but was only 0.70 mM when determined using a 4.6 hr assay.
  • 6.6. Both Km values are lower than reported for similar assays in other molluscs and for most bacteria.
  • 7.7. Effect of substrate preparation on the kinetics are discussed.
  • 8.8. Eight peaks of chitinase activity were resolved by DEAE-Fractogel ion exchange chromatography.
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13.
  • 1.1. Thais haemastoma were transferred from 30 to 15‰ and 15 to 30‰ S and ammonia excretion was measured for 72 hr.
  • 2.2. Increased ammonia excretion following transfer from high to low salinity was significantly greater in snails with the rare Lap allele, Lap94.
  • 3.3. Increased rates of nitrogen loss induced by salinity reductions could be responsible for maintaining the Lap94 allele at low frequency in estuarine populations of T. haemastoma.
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14.
  • 1.1. Total chromophore contents as well as the contributions made by 11-cis retinal were determined by high pressure liquid chromatography in light- and dark-adapted eyes of Orchomene plebs and Glyptonotus antarcticus (Amphipoda and Isopoda, respectively).
  • 2.2. In O. plebs the highest amount of total chromophore in pmol/eye was found to be 18.5 in 36 hr dark-adapted animals. The lowest amount (11.6 pmol/eye) was recorded in 24 hr light-adapted individuals.
  • 3.3. In dark-adapted O. plebs, irrespective of whether dark-adapted for 36 or 60 hr, the percentage of 11-cis retinal was maximally 96.6%. In the light-adapted material it reached 71.2%
  • 4.4. In eyes of 20 hr dark-adapted Glyptonotous antarcticus, possibly because of insufficient dark adaptation, a total chromophore content of only 3.2 pmol/eye was found. The percentage of 11-cis retinal was 55.8.
  • 5.5. Porphyropsin with its testable 3-dehydroretinal (vitamin A2-aldehyde) was not encountered in any of our samples.
  • 6.6. Calculations of photopigment per gram body weight and a comparison with data from freshwater crayfish show that dark-adapted O. plebs possess approximately 20 times the relative photopigment amount of the crayfish. Absolute sensitivity of the eye of O. plebs is, therefore, expected to be very high.
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15.
  • 1.1. Metabolic rates (ml O2/mg/hr) of three geographically separated populations of the carabid beetle Calathus melanocephalus L. (Finse and Je 10y, Norway and Drenthe, The Netherlands) were measured and compared by ANCOVA.
  • 2.2. No significant relationship (P > 0.05) between metabolic rates and body weight or sex of the animals were found.
  • 3.3. Individuals mostly acclimated to low temperatures by increased metabolic rates and in the opposite direction to higher temperatures. Individuals collected in early summer also showed higher metabolic rates than those caught later in the autumn.
  • 4.4. Contradicting the theory of metabolic cold adaptation, beetles from The Netherlands had the highest metabolic rates, beetles from Finse intermediate rates and beetles from Jeløy the lowest rates.
  • 5.5. No significant relation were found between geographical origin of the beetles and their respective chill-coma temperature.
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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. 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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18.
  • 1.1. 14C-dichlorofarnesoate permeated rapidly into Haemonchus contortus (infective juveniles) and Panagrellus redivivus (mixed cultures) and was strongly bound by hydrophobic association (Ks > 10−4M).
  • 2.2. Uptake rose linearly with increases in temperature (5–38°C) and external concentration (C0; 0.07–2.15 × 10−4 M). Within 1 hr the internal concentration, C1 was >C C0.
  • 3.3. The pH of the medium (6–8) did not affect uptake.
  • 4.4. Efflux of dichlorofarnesoate was low: the half-time of release was > 18 hr.
  • 5.5. The uptake curve approximated to the expression C1/C0 = a(1 − e−bt) with a and b as constants and t in hr.
  • 6.6. These results clarify previous work on the inhibitory action of juvenile hormone on the development of nematodes.
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19.
  • 1.1. The mechanism of action of glyburide (a sulfonylurea) on muscle has been investigated by measuring glucose uptake and glucose transporter (GLUT4) protein levels after chronic glyburide treatment.
  • 2.2. A dietary induced insulin resistant rat model (4 wk of high-fat, high-sucrose feeding) was given glyburide (2mg/kg/day) for 10 days and glucose uptake was measured in a perfused hindquarter preparation.
  • 3.3. Protein levels of the GLUT4 glucose transporter were determined by Western analysis.
  • 4.4. After 7 days of treatment, rats fed glyburide had lower blood glucose concentrations 2 hr (72 ± 5 vs 103 ± 12 mg/dl) and 24 hr (97 ± 7 vs 123 ± 7 mg/dl) after glyburide administration with no difference in serum insulin levels compared to vehicle treated animals.
  • 5.5. Glucose uptake was approx doubled in basal state (0 insulin) in response to glyburide (2.8 + 0.4 vs 1.7 ± 0.2μ mol/g per hr).
  • 6.6. Maximal insulin (100 nM) stimulated glucose uptake tended to be higher in the glyburide treated group, but did not reach statistical significance (8.0 ± 0.7 vs 7.0 ± 0.6 μmol/g per hr).
  • 7.7. Western analysis revealed no significant effect of glyburide on the GLUT4 protein level in skeletal muscle.
  • 8.8. These results suggest that glyburide alters glucose uptake through some mechanism other than alterations in the level of the GLUT4 glucose transporter protein.
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20.
  • 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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