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1.
  • 1.1. The effects of photoperiod and pinealectomy on plasma corticoid levels in the goldfish (Carassius auratus) were examined.
  • 2.2. Plasma corticoid levels differed in goldfish maintained under different photoperiod regimes, but this response varied seasonally.
  • 3.3. Pinealectomy altered the effects of photoperiod on plasma corticoid levels but this effect varied with season.
  • 4.4. Plasma corticoid levels were correlated with ovarian activity. The effects of photoperiod on plasma corticoid levels appear to be related to the influence of light on reproduction.
  • 5.5. The alteration of plasma corticoid levels in pinealectomized fish may be due to the role this organ plays in mediating photoperiod effects on gonadal activity.
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2.
  • 1.1.|Resting metabolic rate of laboratory rabbits kept indoors is susceptible to seasonal fluctuations and is higher in winter than in summer.
  • 2.2.|Thermoneutral zone of rabbits under these conditions may shift downwards in winter and upwards in summer.
  • 3.3.|Both of these adjustments in thermoregulation seem to be related to the seasonally changing photoperiod.
  • 4.4.|Dehydration does not influence these thermoregulatory adaptive changes.
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3.
  • 1.1. The participation of an environmental factor such as photoperiod in the metamorphic development of Discoglossus pictus has been studied.
  • 2.2. Short photoperiods were more effective in accelerating the rate of growth and the stages of development of tadpoles than were long photoperiods.
  • 3.3. Daily melatonin injections to tadpoles during larval development showed different effects depending on the artificial photoperiod in which the tadpoles were maintained.
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4.
  • 1.1. The effect of photoperiod on steroid metabolism in Asterias rubens was studied.
  • 2.2. Daylength was artificially shortened in 3 weeks from long-day (LD 18/6) to short-day (LD 6/18) conditions and its effect on the metabolism of pregnenolone and dehydroepiandrosterone was studied in homogenates of gonad and pyloric caeca tissue from male and female seastar.
  • 3.3. Pregnenolone metabolism did not change during the experiment when the animals were kept continuously under the same (long-day) conditions. Pregnenolone metabolism was intensified by decreasing daylength. The production of progesterone reached its maximum at a daylength comparable to that in autumn (LD 12/12), and that of an unidentified steroid at an even shorter daylength.
  • 4.4. Metabolism of dehydroepiandrosterone was influenced by photoperiod. There were indications that androstenedione production is maximal at fall conditions. This was evident for an as yet unidentified steroid.
  • 5.5. Metabolism of DHEA strongly increased during the experiment in animals which were kept continuously under long-day conditions. It is discussed that this may be a reaction to crowding.
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5.
  • 1.1. Metabolic rates and adenine nucleotide content of liver and kidney from hibernating ground squirrels were measured and compared to rats to study the biochemical adaptation to hibernation.
  • 2.2. High rates of renal and hepatic gluconeogenesis were observed in squirrels, particularly from propionate and glycerol compared to rat.
  • 3.3. During hibernation and starvation soluble phosphoenolpyruvate carboxykinase activity was increased in both liver and kidney.
  • 4.4. Although metabolic rates are decreased during hibernation the results suggest that the enzymic complement is maintained at high activity even during torpor.
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6.
  • 1.1. A significant diurnal rhythm of net sodium flux was demonstrated in the freshwater clam Corbicula fluminea entrained to either a 12L:12D or 24L photoperiod.
  • 2.2. Highest net flux occurred during the dark hours on 12L: 12D. The overall mean net flux over 24 hr was not significantly different from a steady state condition.
  • 3.3. Net flux values of clams on a 24L photoperiod were negative and significantly lower than the net flux on a 12L:12D photoperiod.
  • 4.4. The 12L: 12D net sodium flux rhythm pattern is similar to rhythmic patterns of other physiological processes in another freshwater clam.
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7.
  • 1.1. Kinetic aspects of the enzyme UDP-galactose 4-epimerase in crude homogenates of the albumen gland of the snail Lymnae stagnalis were estimated. The mean values of the Km for UDP-galactose and for NAD are 0.343 and 0.097 mM, respectively. The enzyme is inhibited by NADH. It is inactivated by freezing and raised temperature (25°C), but it can be reactivated by NAD.
  • 2.2. In the albumen gland the epimerase activity is 10–100 times higher than in other tissues, reflecting the high turnover of glucose to galactose, essential for the synthesis of galactogen in this organ.
  • 3.3. In fed snails long day conditions stimulates albumen gland epimerase activity, coinciding with high egg production.
  • 4.4. In starved snails a fairly high residual activity of the enzyme is maintained, irrespective of photoperiod or egg production.
  • 5.5. Trematode infection leads to a considerable reduction of the epimerase activity.
  • 6.6. The results indicate that the epimerase activity in fed snails, when the gland shows a regular release, reflects long-term adaptations (photoperiod). In starved and parasitized snails, when no regular release or product occurs, a basic epimerase activity is maintained. This might be important for a rapid restoration of egg production after the termination of adverse conditions.
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8.
  • 1.1. In liver and muscle the concentrations of free amino acids (FAA) are highest in fish maintained at low temperature and fed mealworms. These effects are more pronounced in roach than in rudd.
  • 2.2. In the liver alanine, glycine and glutamate are the dominant FAA but proline increases in mealworm-fed animals.
  • 3.3. In muscle, histidine and glycine dominate, except that a mealworm diet leads to an increase in the concentration of proline and to a concomitant decrease in the concentration of glycine.
  • 4.4. Starvation leads to a reduction of total FAA content but to relative increases of lysine and histidine. These two FAA can serve as indicators of the general state of nutrition of roach and rudd.
  • 5.5. The molar ratio [gly]/[his] is strongly correlated with temperature, decreasing with an increase in the temperature to which the animals had been exposed prior to capture.
  • 6.6. The patterns of free and bound amino acids diverge more widely in these species than in mammals which reflects the greater dependence of the FAA pools of fish on intrinsic and extrinsic factors.
  • 7.7. The concentrations of histidine in the FAA pools of muscle and in food proteins are strongly correlated.
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9.
  • 1.1. In the rat chronic metabolic acidosis increases the net synthesis of 17 renal cortex proteins by amounts ranging from 1.5 to 4.5-fold.
  • 2.2. These proteins have molecular weights between 13,000 and 42,000 and isoelectric points between approximately 5.5 and 7.0.
  • 3.3. No new proteins not also present in normal animals are detected in renal cortex samples from acidotic animals.
  • 4.4. Three proteins undergo substantial reductions in their net synthetic rates in chronic metabolic acidosis.
  • 5.5. On the basis of their physical properties and similar alterations in net synthetic rate in acidosis some of these proteins appear to be closely related and may be coordinately expressed in the rat kidney.
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10.
  • 1.1. The influence of temperature (14,19, 24°C), salinity (26,32, 38,44%.) and food type (artificial diets: Fryfood, Mytilus, Soya, Yeast, Spirulina) on the respiratory rate of Tisbe holothuriae has been studied.
  • 2.2. Oxygen consumption decreased with decreasing temperature, but with a greater rate at supra- or subnormal salinities.
  • 3.3. Multiple-regression analysis showed the quadratic effect of temperature and the linear effect of salinity to be the more important factors affecting respiration.
  • 4.4. The food type also seems to exert an important effect on oxygen consumption.
  • 5.5. A significant lowering of respiration was observed for all food tested when the animals were starved.
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11.
  • 1.1. Glycogen and galactogen contents of the albumen gland of the freshwater snail Lymnaea stagnalis were determined under different conditions, known to influence these polysaccharides viz egg laying, photoperiod and starvation.
  • 2.2. After oviposition, the galactogen content is restored within 32 hr, whereas glycogen remains constant during this period. Short-day photoperiods favour accumulation, long-day photoperiods induce depletion of glycogen. In contrast, the galactogen content is not affected by the photoperiod.
  • 3.3. Since glycogen and galactogen are present in the same cells of the albumen gland, the independent variation of these polysaccharides would imply the presence of separate intracellular regulation mechanisms.
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12.
  • 1.1. Seasonal acclimatization effects on oxygen consumption, body temperature, and body weight were evaluated in three different experimental groups of Dipodomys panamintinus.
  • 2.2. Body weights of wild field as well as captive animals housed in outdoor sand cages were maximum in winter and lowest in summer for both sexes.
  • 3.3. Mean oxygen consumption was maximum in winter and lowest during spring in both sexes of the wild field and captive exposed groups.
  • 4.4. Neither weight nor oxygen consumption of indoor control animals varied with the seasons.
  • 5.5. No significant differences in body temperatures were observed during either the fall or winter seasons.
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13.
  • 1.1. The short-term resting rates of oxygen consumption of laboratory white mice (Mus musculus) and Mongolian gerbils (Meriones unguiculatus) were measured by closed system manometry.
  • 2.2. Metabolic rates of animals tested individually were compared to those of huddled trios and trios in which the animals were tested simultaneously but prevented from physical contact (separated trios) at temperatures ranging from 9–25° C.
  • 3.3. Rates of increase of weight-specific resting metabolism were greatest for animals tested individually.
  • 4.4. There was no significant difference in the rates of increase of oxygen consumption between huddled and separated trios in cither species.
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14.
  • 1.1. Heart rates of adult aquatic red-spotted newts can be conveniently recorded using an impedance pneumograph.
  • 2.2. Heart rates decrease linearly with decreasing temperature.
  • 3.3. Submergence in normoxic and hypoxic water at 10°, 15°, and 20°C results in bradycardia which is more pronounced in hypoxic water.
  • 4.4. At 5°C one newt exhibited the above pattern, but bradycardia was not exhibited by the other newt during normoxic submergence.
  • 5.5. Diminishing heart rates are probably due to oxygen deficiency, not immersion alone.
  • 6.6. Recovery from bradycardia in air is rapid and not linked with resumption of aerial breathing.
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15.
  • 1.1. The temperature and water relations of Centruroides hentzi females were investigated. At 12 and 72% relative humidity (RH), the lower and upper Lt50 were -4.5 and 43.7°C, and -4.7 and 45.1°C, respectively. When exposed to high temperature stress, survivorship was significantly greater under mesic conditions.
  • 2.2. Cuticular water loss was higher under xeric conditions (12% RH), ranging from 0.061 mg/cm2/hr at 30°C to 0.211 at 41°C.
  • 3.3. Exposure to dry air (0–5% RH) resulted in a significant increase in hemolymph osmolality: from 441 to 688 mOsm over a 5 day period.
  • 4.4. Mean oxygen consumption rates increased from 161.7 mm3/g/hr at 34°C to 541.6 at 44°C. ATPase activity was significantly higher in animals acclimated and tested at 35°C.
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16.
  • 1.1.|The standard metabolic rates (SMRs) and preferred body temperatures (PBTs) of the tropical cordylid Cordylus jonesi and temperature lacertid Lacerta lilfordi were determined following acclimation to constant environmental temperatures of 20 and 30°C.
  • 2.2.|Although after 5 weeks the SMRs of Cordylus jonesi and Lacerta lilfordi displayed partial compensations of 20.9 and 10.5%, respectively, their PBTs did not alter over this period. Therefore, acclimation does not maintain complete metabolic homeostasis during either the active or inactive phase of the lizard.
  • 3.3.|Cordylus jonesi allowed to thermoregulate behaviourally at their PBT during activity possessed similar SMRs to control animals maintained continually at the same background temperatures, indicating that acclimation state in lizards is determined by the body temperatures experienced while at rest.
  • 4.4.|The particular acclimatory problems of animals exhibiting behavioural homeothermy are discussed.
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17.
  • 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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18.
  • 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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19.
  • 1.1. Changes in metabolic rates and behavior were observed in tufted titmice (Parus bicolor) and Carolina chickadees (Parus carolinensis) exposed to varying conditions of artificial solar radiation, wind, and temperature in a wind tunnel experiment.
  • 2.2. During the wind-on condition, both species showed a significant decrease in mean metabolic rates in the high radiation treatments when compared to the low radiation treatments (P < 0.05).
  • 3.3. Titmouse orientation, posture and level of activity were significantly affected by radiation and wind conditions.
  • 4.4. Metabolic rates observed in the wind tunnel treatments without wind and at low radiation did not significantly differ from similar standard metabolic (black box) treatments (P > 0.05).
  • 5.5. Activity levels did not appear to directly affect metabolic rates observed in the wind tunnel treatments.
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20.
  • 1.1. After step-like increases in salinity the shrimps exhibit the smallest increase in oxygen consumption in the lower salinity range. At higher salinities the shrimps show longer recovery times and greater increases in the metabolic rate after salinity shock.
  • 2.2. In steady-state experiments, the shrimps display the lowest oxygen consumption rates near the isosmotic point. The lowest metabolic rates occur at salinities of 3‰ and 10‰ At salinities of 20‰ and above the rate of metabolism increases by 20–30%.
  • 3.3. The calculated osmoregulatory work for animals in fresh water amounts to only 2.7% of routine metabolism and drops to 1.1% for shrimps in 3‰ and 0.7% in 5‰ salinity.
  • 4.4. Locomotory activity in the form of position change was not responsible for the increased oxygen consumption of the animals after salinity shocks. A “tentative swimming activity” by fast and frequent beating of the pleopods without position change may be an important factor in the increase of metabolic rates.
  • 5.5. In its temperature response, the brackish water population has a higher metabolic rate than the freshwater one. Between 5 and 35°C Q 10-values range from 4.01 to 1.37.
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