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1.
  • 1.1. The effects of 2% saline imbibition and water deprivation on the water balance of the gerbil were compared.
  • 2.2. The unchanged fluid intake and losses, body weight and several blood indices suggested little alteration in the state of hydration after saline imbibition.
  • 3.3. After 5 days water deprivation the animals lost weight and evidence of haemoconcentration was observed. These changes took place despite reductions in water loss (via the urine and faeces) and evidence of secretion of vasopressin and the two principal acidic neural lobe proteins.
  • 4.4. The gerbil appeared to be better adapted to water stress induced by saline imbibition than by water deprivation and this may be related to its habitat in Northern Asia.
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2.
  • 1.1. Evaporative water loss was measured as a function of temperature, season and grouping in the kangaroo rat, Dipodomys panamintinus for a one year period.
  • 2.2. Three groups of Panamint kangaroo rats were set up and studied during the various changes in season. The three groups were designated as field, exposed and control. These groups revealed the effects of acclimatization, captive acclimatization and laboratory acclimatization respectively.
  • 3.3. There is a highly significant difference in the rate of evaporative water loss in the Field Panamint kangaroo rats during the Fall, Winter and Spring.
  • 4.4. In general, the quantity of water loss via evaporation was higher in the female Panamint kangaroo rats.
  • 5.5. Water loss via evaporation in the control and exposed groups was least affected by seasonal change.
  • 6.6. In comparison to the other two groups, the field male and female Panimint kangaroo rats possessed the highest slope (rate) and mean (quantity) for all seasons.
  • 7.7. The combined effect of both grouping and season affects both the rate and quantity of evaporative water loss in the Panamint kangaroo rat.
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3.
  • 1.1. Metabolism of tritiated water and 22sodium was studied in six beef cows under Mediterranean summer conditions in order to find whether the turnover of these tracers can be used to evaluate pasture intake.
  • 2.2. The diet of the cows included ad libitum access to two components which were given separately in different troughs: one was poultry litter and the other was wheat straw, to simulate the dry pasture.
  • 3.3. Voluntary daily dry matter intake (111 g/kg0.75) was unexpectedly high considering the low digestibility of the feed.
  • 4.4. The assumptions of constant ratios of water intake to water turnover and of dry matter intake to water intake were confirmed. Consequently, dry matter intake was determined accurately from water turnover measurements.
  • 5.5. Sodium intake was practically equal to sodium turnover and most of the sodium secreted in feces was of endogenous origin.
  • 6.6. Pasture intake can be predicted from sodium turnover once the concentration in feed and water consumed is known.
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4.
  • 1.1. The digestive tract was compared with the tract appendages (caeca) in bluegill fish, Lepomis macrochirus in their response to short and long term food deprivation.
  • 2.2. Fasting for 7 days resulted in 80% reduction of food content in the main tract, but only 40% reduction in appendages (caeca).
  • 3.3. The intestine exhibited two different patterns of food distribution under fed and food deprived conditions.
  • 4.4. The histopathological impact of starvation was more prominent on the intestine than on caeca.
  • 5.5. These results suggest that digestive tract and appendages concommitantly conserve food during food scarcity, but appendages may offer advantages in retaining food longer, and in their greater resistance to starvation-induced effects.
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5.
  • 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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6.
  • 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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7.
  • 1.1. Some aspects of the gas exchange system of a diving lizard, Physignathus lesuewii were studied.
  • 2.2. Breathing patterns were analysed.
  • 3.3. Breathing rate increases logarithmically with temperature and Q10 = 1.8. LogBR = −0.237 + 0.0256 T.
  • 4.4. Gas tensions in lung air and arterial and venous blood were measured. Arterial pH declines with increasing temperature.
  • 5.5. Temperature has a marked effect on oxygen affinity of the blood (ΔH = −10.1 kcal mol). A Bohr effect was also noted.
  • 6.6. CO2 equilibrium curves were drawn.
  • 7.7. The results are considered with a view to anticipating the efficiency of the gas exchange system of this species under conditions of variable temperature and during diving.
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8.
  • 1.1. The ECG of aquatic Amhystoma tigrinum from the Colorado Rocky Mountains was recorded while the animals submerged and emerged in water. Older larvae and metamorphosed adults were compared.
  • 2.2. Free-swimming animals of both types showed slight emergence tachycardia when taking a “gulp” of air.
  • 3.3. Preventing access to air for 30 min or more resulted in a slight bradycardia in larvae. Some adults responded with increased, others with decreased, heart rate depending on their level of excitement.
  • 4.4. Restraining the animals before forced submergence caused a greater bradycardia than when unrestrained.
  • 5.5. Low dissolved oxygen accentuated the cardiac responses of larvae to submergence but not in adults.
  • 6.6. Atropine only partially blocked the diving responses of both forms.
  • 7.7. The degree of submergence bradycardia seems to be a function of the ability to extract oxygen from water. It probably is not an adaptation to diving in these forms. Instead the submerged heart rate in these predominantly aquatic salamanders may be the “normal” rate with emergence tachycardias for breaths of air.
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9.
  • 1.1. The effects of thermal acclimatization at 10 and 24°C on heart rate were investigated on unrestrained soles (Solea vulgaris).
  • 2.2. The sensitivity of heart rate to temperature changes induced by temperature acclimatization was higher in cold-acclimatized than in warm-acclimatized soles.
  • 3.3. Heart rate of cold-acclimatized fish to temperature changes was not affected by blocking the vagal tone with atropine.
  • 4.4. After atropine treatment the ability of heart rate to show thermal compensation decreased in warm-acclimatized soles.
  • 5.5. It is suggested that the vagus nerve can function differently at different temperatures.
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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. Coatis are chiefly diurnal, showing marked nycthemeral variations of body temperature and oxygen uptake.
  • 2.2. The thermoneutral zone extends from 25–33°C; the basal metabolic rate is about 40% below the value predicted from body mass.
  • 3.3. Thermoregulation in cold is excellent, partly due to decreasing thermal conductance at falling ambient temperatures.
  • 4.4. Exposure to temperatures above 35°C is endured for only short periods.
  • 5.5. Basal heart rate is reduced to about 70% of the predicted level. The contribution of heart rate to increased oxygen demands at falling ambient temperatures is rather low.
  • 6.6. The measured physiological characteristics of coatis are discussed with regard to the high mobility and the wide distribution range of these procyonids.
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12.
  • 1.1. Three monoclonal antibodies have been produced which neutralize in vitro the haemolytic activity present in tentacle extracts of the box jellyfish (Chironex fleckeri).
  • 2.2. Two of these monoclonal antibodies bound specifically to a component of relative molecular mass 50,000 in tentacle extract on Western blots.
  • 3.3. This binding only occurred when the extracts were electrophoresed under non-reducing conditions.
  • 4.4. The third monoclonal antibody did not display binding to Western blots of tentacle extract under any of our experimental conditions.
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13.
  • 1.1. Ultradian oscillations in the min and hr range on long-term (24-hr) computerized recordings of heart rate in rainbow trout Oncorhynchus mykiss, acclimated to 5, 10 and 15°C water temperature, were investigated. Eight-hour duration time series derived from the heart rate recordings were analysed for their harmonic content in the ultradian band by spectral analysis.
  • 2.2. A significant ultradian rhythm at around 0.011 cycles/min (approximately 91-min period) was detected in the power spectral density functions of all the 8-hr duration time series derived from the heart rate recordings at the three experimental water temperatures.
  • 3.3. The spectral power of the ultradian oscillation detected in heart rate of trout was found to increase significantly with increasing temperature.
  • 4.4. The possible endogenous origin of the ultradian rhythm detected in heart rate of Oncorhynchus mykiss is discussed.
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14.
  • 1.1. The role of the visceral nerve in mediating the changes in heart rate associated with different behavioral patterns was investigated in Megalobulimus sanctipauli.
  • 2.2. The results of acute and chronic denervation experiments indicate that the visceral nerve has no excitatory or inhibitory tonic action on the heart of snails retracted into the shell, nor does it account for the increase in heart rate associated with the locomotion and feeding behaviors.
  • 3.3. These changes in heart rate are, probably, indirect effects of increased activity such as an increase in venous return.
  • 4.4. The visceral nerve is responsible for approximately 3/4 of the increase in heart rate associated with the first minute of extrusion.
  • 5.5. The small increase in heart rate observed in denervated animals is probably caused by an increase in venous return generated by muscle activity that forces the head and food out of the shell.
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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. 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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17.
  • 1.1.Responses to different salinities monitored by opening and closing of the shell valves were observed in Modiolus fluviatilis.
  • 2.2.The osmotic pressure, sodium and chloride ion concentrations were measured in the haemocoelic fluid of Modiolus fluviatilis under similar conditions.
  • 3.3.Free amino acids (measured as ninhydrin-positive substances) were determined in the muscle tissue of Modiolus.
  • 4.4.It appears that these free amino acids are involved in the ability of the estuarine bivalve Modiolus fluviatilis to osmoregulate in a wide range of salinities.
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18.
  • 1.1. Observation of ventilation in immersed Pholis gunnellus showed a linear relationship between ventilatory rate and temperature between 8 and 20°C.
  • 2.2. At 13°C and after 30 min emersion, ventilatory rate was initially lower than prior to emersion, providing evidence of adequate uptake of O2 for standard metabolism during the emersion period.
  • 3.3. This species has a laterally elongate body form with reduced scales and extensive mucus secretion.
  • 4.4. During emersion, gaping behaviour probably exposes the gills and extensively vascularised oesophageal regions to air.
  • 5.5. These are considered to be morphological and behavioural adaptations by P. gunnellus, to aerial respiration in the intertidal habitats occupied by this species.
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19.
  • 1.1. Steady state data was obtained for alkaline phosphatase over a wide range of experimental conditions using two substrates, four inhibitors, two modifiers and several pH, ionic strength and temperatures values.
  • 2.2. The data was fitted by rational functions of degree 1:1, 2:2 and 3:3 using a non-linear regression program and then the F-test was used to assess the goodness of fit.
  • 3.3. A proportion of the curves could only be fitted by 2:2 functions but many of them could be adequately fitted by 1:1 functions.
  • 4.4. No statistically significant improvement in fit occurred with 3:3 functions.
  • 5.5. Data was simulated using a computer program to see what sort of curves could be generated by a two sites mechanism proposed for alkaline phosphatase and this study showed that it is difficult to detect cubic terms in this rate equation.
  • 6.6. It was concluded that alkaline phosphatase does not obey Michaelis-Menten kinetics. Rather, the steady state data require a mechanism of at least second degree but do not exclude a rate equation of third degree.
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20.
  • 1.1. Bullfrogs were maintained in air-saturated water at 4°C under an 8:16hr, light:dark, photoperiod for 50 days from December to February.
  • 2.2. Heart rates and mean arterial pressures from these submerged frogs remained stable throughout the entire period in the cold. The slow heart rates that were observed appeared to result from a combination of low temperature and submergence. No indication of torpor was observed in any of the animals.
  • 3.3. These findings demonstrate that the cardiovascular system of bullfrogs apparently retains normal regulatory function when these animals are maintained under temperature and photoperiod conditions analogous to those found during overwintering.
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