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1.
  • 1.1. Measurements of aerobic scope (resting and active oxygen consumption rates) and anaerobic scope (resting and active production of lactate rates in the whole body homogenates) were carried out on the desert skink, Chalcides ocellatus at temperatures between 10 and 40°C.
  • 2.2. The aerobic scope was maximal around the preferred body temperature with a low thermal temperature dependence above the preferred levels.
  • 3.3. During initial stages of forced activity, C. ocellatus employed anaerobic metabolism as its major energy source.
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2.
  • 1.1. Common carp (Cyprinus carpio) exposed to experimental temperatures of 12, 18, 24, 30 or 36°C for a 4-week period were used to investigate the effect of temperature acclimation on the frequency of opercular movement (FOM), growth and cytochrome c oxidase (CCO) activity in heart, liver and muscle.
  • 2.2. An exponential relationship between FOM and temperature after the first week (1010 =1.76) disappeared after the second week.
  • 3.3. The initially high FOM at temperatures of 30 or 36°C and the low FOM at 18 or 12°C changed over 4 weeks to approach the FOM of fish at 24°C.
  • 4.4. This change in the relationship of FOM to temperature from highly dependent to independent appeared to be thermal compensation.
  • 5.5. Heart and liver CCO activities were significantly affected by temperature, with the lowest activity at the approximate optimum temperature for growth, 24°C.
  • 6.6. Highest CCO activities for heart and liver occurred at both the highest and lowest temperatures.
  • 7.7. Among the three tissues, heart CCO activity was generally the highest and most affected by acclimation temperature.
  • 8.8. Muscle tissue had the lowest CCO activity and was unaffected by temperature.
  • 9.9. The high CCO activity at a cold acclimation of temperature 12°C was probably due to thermal compensation and the high activity at 36°C may have been a result of thermal stress.
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3.
  • 1.1. The oxygen consumption of Bullia digitalis from South Africa's west coast, measured at a fixed activity level at 15°C, does not differ significantly between winter and summer.
  • 2.2. The adult acute rate-temperature curve is flattened over the temperature range likely to be encountered in the field, there being no significant difference in oxygen consumption between 15 and 22.5°C.
  • 3.3. Below this plateau the Q10 is normal, giving a value of 2.67 between 5 and 10°C, but at temperatures above 22.5°C the Q10 is less than 2 and oxygen consumption at 30°C does not approach that of the tropical Bullia melanoides at the same temperature.
  • 4.4. Both field and laboratory acclimated animals provide evidence that the rate-temperature curve is unaffected by such acclimation, either to high or low temperatures.
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4.
  • 1.1. Oxygen consumption at 18°C was 60% of the rate at 22 and 26°C.
  • 2.2. Critical points, where the rate of oxygen consumption changed, were defined at 22°C (2.89 mg DO) and 26°C (3.46 mg DO). Linear regressions were fitted showing that oxygen consumption declined significantly (81.5% ±4.5) below the critical point.
  • 3.3. Oxygen consumption was proportional to weight. Allometric relationships resulted in variable temperature-related coefficients for respiratory dependence on weight, a reflection of the crayfish adaptation towards re-establishment of a new equilibrium state.
  • 4.4. Heart beat rate was lower at 18°C, and highest at the acclimation temperature (22°C). Stress at 26°C was evident.
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5.
  • 1.1. The exponent (b) relating metabolic rate to dry weight in excised gills of Tagelus plebeius is not maintained constant throughout the seasons or upon acute exposure to temperatures of 9–34°C.
  • 2.2. Acclimation (11–29°C) and test (9–34°C) temperatures have a significant effect (α = 0.01) on the mean rate of oxygen uptake by the gills.
  • 3.3. Positive seasonal thermal acclimation is observed up to acclimation temperatures of 19.5–20°C, which is also the temperature of minimum respiratory response to all acute test temperatures.
  • 4.4. Regions of thermal metabolic insensitivity are seen over small acute temperature ranges near the acclimation temperatures.
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6.
  • 1.1. The detection of G6PD and 6PGD in A. proteus can be used to investigate the functioning of the phosphogluconic (or pentose phosphate) pathway in these amoebae.
  • 2.2. In amoebae cultured at 10°C compared with those kept at 25°C, no differences in the number of G6PD, 6PGD and GlcDH electromorphs are revealed.
  • 3.3. The acclimation of amoebae cultured at 25°C to a relatively low temperature of 10°C is accompanied by an increase in the activities of total Triton-soluble G6PD, 6PGD and GlcDH per cell, a rise in the activity of GlcDH per unit cell protein, and a change in the activity and heat resistance of some G6PD electromorphs.
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7.
  • 1.1. Active transport of d-glucose was shown using intestinal sac preparations, in vitro, made from two marine fish, the scup, Stenotomus versicolor and the puffer, Spheroides maculatus.
  • 2.2. Differences in absorption characteristics were evident in populations from year to year.
  • 3.3. Anaerobiotic conditions, i.e. 100 per cent nitrogen gassing of the incubation medium, inhibit the active transport of d-glucose in scup and puffer intestine.
  • 4.4. Phlorizin, 5 × 10−4 M, inhibits the active transport of d-glucose in scup intestine.
  • 5.5. Intestinal transmural glucose transport mechanisms operate well at incubation temperatures, 20°–27°C, i.e. temperatures close to habitat and holding tank temperatures, whereas movement of the sugar against a concentration gradient is interrupted at higher incubation temperatures, 29° and 30°C.
  • 6.6. Detailed comparison of procedures and results with those used by other workers in the field of in vitro intestinal absorption of poikilotherms suggests that aerobic metabolism may not be a uniformly significant energy source in intestinal active transport.
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8.
9.
  • 1.1. Cardiac frequency patterns of Callincctes sapidus Rathbun were used to evaluate potential thermal stress after exposure to 5°C increases over a range of acclimation temperatures from 5° to 30°C.
  • 2.2. An acclimated rate-temperature curve (R-T curve), acute R-T curves of the stabilized rates at the increased temperatures and Q10 temperature coefficients were used to assess the significance of the changes in rate frequency.
  • 3.3. The acclimated R-T curve showed that blue crabs go through a series of seasonal adaptation types characterized by a plateau of perfect adaptation for both cold and warm adapted organisms. Paradoxical adaptation occurred between the transition from cold to warm acclimation temperatures.
  • 4.4. The acute R-T curves showed that cardiac frequency was highly responsive to a 5°C increase when the organisms were acclimated to low temperatures.
  • 5.5. The Q10's of the acute R-T curves at the warm acclimation temperatures approximated those values derived for the acclimated R-T curve.
  • 6.6. This suggests that the temperature increase had a negligible effect on the warm adapted crabs, that is, little or no thermal stress occurred.
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10.
  • 1.1. The effect of acclimation to 10° and 30°C on the blood volume, clotting time, total blood protein and numbers of cells was determined in Uca pugilator.
  • 2.2. There was no significant difference between blood volume in the 10° and 30° animals but there were significantly more cells and a higher blood protein in the 30° crabs.
  • 3.3. The clotting time is significantly longer for the 10° crabs.
  • 4.4. These changes associated with the blood parameters can be associated with the ecology of the animal.
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11.
  • 1.1. The effect of short-term (79 hr) food deprivation at 27°C on body mass, locomotor activity, body temperature (Tb), and resting oxygen consumption was determined in eleven American kestrels (Falco sparverius).
  • 2.2. The change in body mass during resting followed the relation, % mass remaining = 99 e0.07(days fasting). There was no significant difference in the rate of relative mass loss between males and females.
  • 3.3. Locomotor activity, measured as perch hopping, was highly variable in both control and fasted birds and showed no correlation with stage of the fast, basal metabolic rate (BMR), or rate of mass loss during food deprivation.
  • 4.4. Body temperatures of fasted birds declined continuously by 0.2–0.4°C per day from 39.3 to 38.3°C.
  • 5.5. Both males and females responded to food deprivation with a decrease in metabolism. By the third night of fasting, BMR had declined 23.4% from 0.845 W (bird day)−1 to 0.647 W (bird day)−1. The observed reduction in BMR is 2.4 times that expected from a 1°C decline in Tb (assuming Q10 = 2.5) indicating active suppression of metabolism.
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12.
  • 1.1. Activities of the red and white muscle LDH from 8°C-acclimated goldfish were about three times higher than those acclimated to 28°C.
  • 2.2. Isozyme composition and some kinetic properties of the red muscle LDH differed from those of the white muscle enzyme.
  • 3.3. The amount of red muscle as well as LDH activity tended to increase during cold acclimation.
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13.
  • 1.1. The effect of cold (8 ± 2°C) acclimation on the lactate dehydrogenase activities and isoenzyme patterns from sartorius muscle, liver, heart and brain of adult Discoglossus pictus pictus (Otth.) was studied.
  • 2.2. Two groups of animals were studied: one set of animals was trapped in October and another set in December. In both cases some of the animals were sacrificed upon collection and some others subjected to 5 months of acclimation at 8 ± 2°C before being sacrificed for analysis.
  • 3.3. A general trend towards a decrease in LDH specific activity was observed during cold acclimation. The magnitude of change, but not the direction, depends on both the tissue examined and the season at which the experiment was initiated.
  • 4.4. A complex LDH isoenzyme reorganization was also found in liver, heart and brain. In liver from Experiment 1 and in heart from both experiments, a relative maintenance in M-type LDH activity during cold acclimation was observed. However, in brain there was a relative maintenance of LDH3 activity in both experiments.
  • 5.5. The low behavioral activity (and its metabolic consequences) and the existence of an intrinsic annual rhythm in D. pictus metabolism are suggested as responsible for the observed enzymatic changes.
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14.
  • 1.1. Mortality was 100% at pH 3.5 over a temperature range of 10–30°C for embryos and nymphs of Caenis diminuta and C. hilaris.
  • 2.2. Hatching success for both species was highest at pH values above 4.5.
  • 3.3. Survival capacities were significantly higher at 20°C over a pH range of 4.0-7.2.
  • 4.4. Oxygen consumption rates increase as a function of increasing temperature and reduced acidity.
  • 5.5. Loss of the nymphal righting response was observed at pH 3.5. This response can be used as a behavioral assay for acid stress.
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15.
  • 1.1. Differential thermal acclimatory responses of maximal catalytic rates (Vmax) of digestive enzymes have been measured in both sexes of Periplaneta americana adapted to 16 and 32°C.
  • 2.2. Salivary amylase of females and gastric protease of males exhibit “translational” acclimation, the former showing a “complete” but the latter only a “partial” compensation. The value of Q10 is not altered in the adaptive response.
  • 3.3. An alteration of the thermal coefficient is evidenced by the “translational-cum-rotational” compensation of gastric amylolytic activity, with significant warm acclimation but no cold acclimation in both sexes.
  • 4.4. Gastric protease of female cockroaches and gastric lipase of both sexes are characterized by the lack of an adaptive compensation to temperature, while salivary amylase of male appears to manifest an “inverse” acclimation.
  • 5.5. Sexual dimorphism in the levels of the activities and in the patterns of thermal acclimation of the digestive enzymes is indicated.
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16.
  • (1)The preferred temperatures of Macrobrachium acanthurus were determined for prawns acclimated to 20°C, 23°C, 26°C, 29°C and 32°C, and the final preferendum estimate was (29.5°C).
  • (2)The critical thermal minima (CTMin) and maxima (CTMax) were 11.0°C, 12.1°C, 13.0°C and 14.8°C, and 34.2°C, 35.0°C, 36.1°C and 39.8°C, respectively.
  • (3)The zone of thermal tolerance assessed using the CTMin and CTMax boundaries was 644°C2.
  • (4)The acclimation response ratio was between 0.33 and 0.62.
  • (5)To cultivate this species in the southeastern region of México it should be done in not <15°C (CTMin) during the winter and below 38°C in summer (CTMax).
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17.
  • 1.1. A respirometer for long-term measurements of oxygen consumption in terrestrial vertebrates is described.
  • 2.2. The tortoise, Testudo hermanni Gmelin, investigated in summer and autumn, presents a day-night rhythm of oxygen consumption at 28 and 18°C but not at 8°C.
  • 3.3. The standard metabolic rate presents an important and constant thermal dependence in the range 8-18-28°C.
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18.
  • 1.1. Heart rate-temperature relationships were determined on unanaesthetized, unrestrained eels acclimated to 15°C and 25°C.
  • 2.2. Heart rate in eels with intact vagal tonus exhibited a nearly complete temperature compensation. The degree of compensation was considerably reduced by blocking the vagus function with benzetimide.
  • 3.3. The difference in the sensitivity of heart rate to temperature change induced by temperature acclimation was significantly decreased after benzetimide-treatment.
  • 4.4. The inhibitory vagal tonus was significantly higher in warm-acclimated than in cold-acclimated eels.
  • 5.5. It is concluded that adaptation of heart rate to temperature is mediated by the parasympathetic system to a great extent.
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19.
  • 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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20.
  • 1.1. Proteolytic, lipolytic, amylolytic and cellulolytic activities were studied in adults of the phytophagous beetle, Hydromedion sparsutum, indigenous to the sub-Antarctic island of South Georgia.
  • 2.2. Gastric enzyme activities were measured at experimental temperatures of 5–40°C and results were compared with those obtained from two thermophilic insects, Gryllus bimaculatus and Tenebrio molitor.
  • 3.3. Protease and lipase activities in Hydromedion were 10–15 times lower than in Gryllus and Tenebrio.
  • 4.4. In the temperature range of 5–15°C, α-amylase activity from Hydromedion was only slightly lower than that from Gryllus.
  • 5.5. Hydromedion gut homogenates exhibited a distinct cellulolytic activity, even at a low temperature of 5°C.
  • 6.6. Cellulolytic activity in the digestive tract of Hydromedion was confirmed by the evolution of 14CO2 after consumption of labelled cellulose.
  • 7.7. The thermal properties of digestive enzymes agree well with the role of Hydromedion as primary decomposer in its ecosystem.
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