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1.
  • 1.1. Malleefowl Leipoa ocellata have a lower than predicted metabolic rate, a finding common to many arid adapted avian species.
  • 2.2. Evaporative water loss was as expected by allometric analysis. However, in the wild this species probably reduces its evaporative water loss because their water turnover rate is extremely low.
  • 3.3. Malleefowl coped with temperatures up to 40°C well, but above this temperature they become highly agitated.
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2.
  • 1.1. The house sparrow, Passer domesticus, has a circadian rhthym of metabolism and body temperature.
  • 2.2. Evolutionary adaptation to a hot and humid climate is reflected in the lower metabolism and greater insulation of the Houston population than observed in populations from Ann Arbor, Michigan; Boulder, Colorado and Syracuse, New York.
  • 3.3. There are no significant differences in either body temperature or evaporative water loss of all four populations.
  • 4.4. The Houston population is able to survive higher ambient temperatures than is found in the Ann Arbor, Michigan or Boulder, Colorado population.
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3.
  • 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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4.
  • (1)We designed a physical model that simulates the thermal and evaporative properties of live Western toads (Bufo boreas).
  • (2)In controlled tests, the model tracked the body temperature of live toads with an average error of 0.3±0.03 °C (test range=4–30 °C).
  • (3)It estimated the evaporative water loss of live toads with an average error of 0.35–0.65  g/h, or about 14% (test range=0.7–9 g/h).
  • (4)Data collected with this physical model should provide an effective way for biologists to better understand habitat selection in toads and other amphibians
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5.
  • 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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6.
  • 1.1. The behaviour of the tRNA population during the acclimatization process was studied, examining the intracellular levels of aminoacylated-tRNAs in livers from summer and winter adapted carps (Cyprinus carpio).
  • 2.2. The in vivo content of Val-tRNA, Ala-tRNA and Met-tRNA decreased significantly during the summer season, in which Val was 80%, Ala 47% and Met 54% with respect to the values attained in winter.
  • 3.3. The half-life for the nonenzymic deacylation showed significant variations for the two populations of aminoacyl-tRNA obtained from summer and winter acclimatized fish.
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7.
  • 1.1. The haematology of tame racing pigeons (Columba livia) and wild guinea-fowl (Numida meéagris) was investigated immediately after transportation to the laboratory and during subsequent acclimatization.
  • 2.2. Significant changes were observed in many of the parameters studied and both experimental groups showed similar variations.
  • 3.3. The results are discussed in relation to the factors which may be responsible for incorrect haematological values being obtained in birds.
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8.
  • 1.1. Haemolymph volume decreases during the initial 16 hr post-ecdysial period, increases after water ingestion and subsequently drops until the inter-ecdysial level is reached.
  • 2.2. Total body water follows a similar pattern, but the changes are not as pronounced.
  • 3.3. Tissue water is inversely proportional to the total body water.
  • 4.4. Soluble cuticle protein declines throughout the initial 16 hr period while both β-glucosidase and alkaline phosphatase activity is lost within 6 hr after ecdysis.
  • 5.5. Dehydration of the cuticle also occurs during the immediate 6 hr post-ecdysial period.
  • 6.6. These data suggest that the formation of the protein-insoluble matrix is linked with water loss.
  • 7.7. Water removal may decrease the distance between molecules allowing specific reactions to take place.
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9.
  • 1.1. Small crabs survived over 18% water loss and large crabs 21% when in dry air. Size, temperature and relative humidity affected this rate.
  • 2.2. Haemolymph osmolarity of newly collected crabs ranged from 530 to 630 mOsm/kg, depending on their size and the season.
  • 3.3. When dehydrated, haemolymph osmolarity rose to over 700 mOsm/kg, and ion concentration increased by over 10%.
  • 4.4. Crabs survived in sea-water for at least two weeks. Haemolymph osmolarity rose and ion concentration increased. The acclimation pattern affected the haemolymph osmolarity.
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10.
  • 1.1.The study was designed to determine if there are sex-dependent differences in vascular reactivity to adrenergic agents.
  • 2.2.Vascular reactivity of both aortic and tail artery smooth muscle from male and female rats to various vasoactive agents was assessed. 3.li]The vascular response of aortic smooth muscle to both phenylephrine and isoproterenol were significantly greater in male rats as compared to females.
  • 3.4.There were apparent sex differences in responsiveness to the KCl-induced, non-receptor mediated contraction of aortic smooth muscle in that the sensitivity to KCl was enhanced in male rats.
  • 4.5.No sex differences were observed in tail artery preparations.
  • 5.6.Phentolamine reduced the maximal tension induced by KCl in the tail artery but not aortic artery preparations. This effect was not sex dependent.
  • 6.7.No differences in the vascular smooth muscle responsiveness to acetylcholine or sodium nitrate was observed between groups or within different vascular beds.
  • 7.8.The increased sensitivity of males to adrenergic challenge could explain in part some of the existing sex differences in cardiovascular disease and hypertension.
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11.
  • 1.1. The urate, urea and ammonia content of the whole egg of the Japanese quail was measured in late incubation in eggs subject to different rates of water loss.
  • 2.2. High rates of water loss substantially increased egg urate content, but had little or no effect on urea or ammonia content.
  • 3.3. Allopurinol, an inhibitor of urate synthesis, reduced egg urate content to low levels, but produced no effect on urea content, and a small reduction in ammonia content.
  • 4.4. The urea concentration of the embryo was lower than in allantoic fluid.
  • 5.5. It is concluded that urate production by the avian embryo is primarily concerned with the modification of allantoic fluid composition.
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12.
  • 1.1. Norepinephrine-induced lipolysis, cyclic AMP production and glycerokinase activity were measured, in vitro, in the brown fat of rats born and reared at either 28° or 16°C during the first 3 weeks of life.
  • 2.2. During the first two postnatal days, lipolytic activity in the tissue was lower than in the foetuses at both ambient temperatures At day 10, increased values of the parameters under consideration were similarly observed in both groups.
  • 3.3. However, the hormonal regulation of lipolysis seemed to be quite different from that found in adult cold-acclimated rats.
  • 4.4. At day 21, the cold-induced characteristics of lipid metabolism in brown fat were observed in the 16°C exposed rats, whereas a loss of tissue stimulation occurred in the 28°C exposed ones.
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13.
  • 1.1The glutathione S-transferase activity in hepatopancreas of the American red crayfish Procambarus clarkii after 15 days' acclimatization in tap water aquaria was measured in specimens collected monthly for a whole year, and shows seasonal variation.
  • 2.2. Previous data on the environmental pollution of Lake Albufera suggest a possible correlation with the activity tested in the different seasons of the year considering the results of non-acclimatized animals.
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14.
  • 1.1. Growing male kittens were fed an 18% casein diet supplemented with 2, 3, or 4% l-methionine (MET) for 6 weeks.
  • 2.2. Free MET concentration in liver increased 30-fold and cystathionine two- to three-fold; the activity of adenosyl-MET transferase and cystathionase also increased but remained lower than previously found in rats.
  • 3.3. Taurine concentration in liver decreased in cats fed excess MET and appeared to depend on taurine intake.
  • 4.4. Alanine aminotransferase activity was high in all groups while serine dehydratase activity was very low.
  • 5.5. Pyruvate kinase and malic enzyme activities which are normally low in cat liver increased after excess MET. Also, glucose 6-phosphate and 6-phosphogluconate dehydrogenases increased.
  • 6.6. Cat liver metabolism showed limited adaptation to an excess dietary intake of methionine compared to that found in rats.
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15.
  • 1.1. Hatching Caretta caretta may lose up to 12% of their initial hatched weight from water loss during emergence from the nest.
  • 2.2. After subsequent osmotic and excretory water loss in sea water, hatchlings will drink sea water (166 μl 100 g−1 hr−1) and return to their initial weight within 10–15 days, without feeding.
  • 3.3. There were no significant changes in plasma osmolarity or sodium levels over this period.
  • 4.4. This osmoregulatory strategy is in marked contrast to that seen in the estuarine crocodile, Crocodylus porosus.
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16.
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Highlights
  • •Efficient sample preparation workflow for deep N-glycomics analysis from serum.
  • •Temperature gradient denaturing protocol to prevent protein precipitation.
  • •Decrease of free sugar content in serum enhanced PNGase F digestion efficiency.
  • •Modified evaporative labeling method increased fluorophore labeling yield.
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17.
  • 1.1. The salinity tolerance in young RS × B hybrids increases as the fingerlings grow. The specimens weighing about 7 g are able to tolerate the direct transfer to the water salinity 18%..
  • 2.2. Under hypo- and iso-osmotic water ion concentration in the hybrid muscle free amino acids, the exchange of taurine for β-alanine and glycine takes place.
  • 3.3. Under hyperosmotic conditions within the first 2 days in the hybrid muscle the water quantity declines, the protein quantity also slightly decreases, the urea and free amino acids concentration (mostly alanine, aspartic and glutamic acids, leucine), and a portion of reserved lipids increase.
  • 4.4. During the next 4 days the muscle moisture, protein quantity, and the concentration of urea and free amino acids return to control values, but the portion of reserved lipids declines below the original level.
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18.
  • 1.1. Potassium loss occurs through the gills of trout.
  • 2.2. This loss is compensated by intestinal absorption.
  • 3.3. During a fasting period, branchial regulation appears after 2–3 days.
  • 4.4. The maintenance of potassium balance is discussed as a function of experimental conditions.
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19.
  • 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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20.
  • 1.1. Rates of water loss in Megetra cancellata were very high compared to those reported for other xeric arthropods.
  • 2.2. Hemolymph weight in hydrated animals was 43.0% of the total body weight while it was 24.7% in desiccated animals that had lost 16.1% of their body weight as water.
  • 3.3. Hemolymph osmotic potential increased from 417 to 447 mOsm/kg in desiccated beetles, but osmotic regulation was evident.
  • 4.4. Total hemolymph protein mass and concentration decreased in desiccated beetles while amino acid concentrations remained constant (at about 70 mM).
  • 5.5. Na+ and −PO4 concentrations increased in desiccated beetles.
  • 6.6. Cl and K+ concentrations in desiccated beetles were equal to those in undesiccated beetles.
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