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1.
  • 1.1. Hemolymph osmoregulation was examined in Chrysochus auratus, Tetraopes tetrophthalmus and Tenebrio molitor. These beetles differed in their water loss rates and in the availability of free water in their habitats.
  • 2.2. During dehydration at comparable rates, osmotic responses were similar in these species. Osmoregulation after rehydration was better in C. auratus.
  • 3.3. Osmoregulation ability was not significantly affected by the beetle's rate of dehydration.
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2.
  • 1.1. Carp red cells were treated with drugs that affect the cell membranes. The water content of the cells and the accumulation of cAMP in the cells were measured in normoxia and in hypoxia using non-stimulated and adrenergically stimulated cells.
  • 2.2. WGA, DIDS + CCCP and A23187 increased the water content of nonstimulated normoxic cells.
  • 3.3. In hypoxia ouabain and DIDS + CCCP increased the water content but cytochalasin B, NPM, DIDS, CCCP and A23187 + CA2+ abolished the hypoxia-induced swelling.
  • 4.4. Any membrane perturbation induced some cAMP formation, Sophora and Anquilla lectins being most potent.
  • 5.5. Also in adrenergically stimulated cells, membrane perturbation generally increased cAMP formation.
  • 6.6. However, cAMP accumulation diminished in cells treated with cytochalasin B, CCCP and DIDS + CCCP.
  • 7.7. The adrenergic swelling of carp red cells was reduced in normoxia by DIDS. NPM and CCCP increased the adrenergic swelling in normoxia to hypoxic level.
  • 8.8. In hypoxia WGA and Anquilla lectin decreased the swelling.
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3.
  • 1.1. Both the small riparian skink Sphenomorphus quoyii and its completely terrestrial relative Ctenotus robustus respond to forced submergence with instantaneous bradycardia.
  • 2.2. The strength of the bradycardia was affected by water temperature and fear. Dives into hot (30°C) water produced weak and erratic bradycardia compared to dives into cold (19.5°C) water. For S. quoyii the strongest bradycardia occurred when submergence took place in water at a lower temperature than the pre-dive body temperature.
  • 3.3. Upon emergence both species of skink exhibited elevated heart rates and breathing rates while heating from 19.5 to 30°C, compared to heating at rest. The increased heart and breathing rates probably act to replenish depleted oxygen stores and remove any lactate. Increased heart and ventilation rates are not indicators of physiological thermoregulation in this case.
  • 4.4. Both lizard species exhibited higher heart rates and ventilation frequencies during heating than cooling.
  • 5.5. Compared to its terrestrial relative, S. quoyii does not appear to possess any major thermoregulatory, ventilatory or cardiovascular adaptations to diving. However, very small reptiles may be generally preadapted to use the water to avoid predators.
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4.
  • 1.1. The oxygen consumption of red and green Carcinus in normoxic and hypoxic sea water was determined, using an oxygen electrode in a sealed respirometer.
  • 2.2. The red crabs had significantly higher “excited” oxygen uptake rates and a lower ability to compensate for hypoxia than the green crabs.
  • 3.3. Red Carcinus display an emersion response to declining oxygen at lower oxygen tensions than the green crabs.
  • 4.4. Mortality of red crabs exposed to prolonged anoxia was much greater.
  • 5.5. The relationship of these findings to the zonation of the two colour forms on the shore is discussed.
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5.
  • 1.1. Uptake and elimination of lindane, 3,4-dichloroaniline, phenol and 4-nitrophenol by the zebrafish Brachydanio rerio were investigated in tap water and in water of the river Rhine.
  • 2.2. The differences in bioconcentration of chemicals between the two water types did not exceed a factor of 2.5.
  • 3.3. Elimination kinetics were comparable in tap and river water.
  • 4.4. It can be concluded that water of the river Rhine does not influence the kinetics of the investigated xenobiotics.
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6.
  • 1.1. Mitochondria with high respiratory control ratios (RCR) have been isolated from the ventricle of the marine clam Mercenaria mercenaria.
  • 2.2. Proline is the preferred substrate of the mitochondria of the ventricle based on state 3 rates.
  • 3.3. Pyruvate, ornithine and succinate are oxidized at rates 3/4 that of proline.
  • 4.4. α-Glycerophosphate was oxidized at rates 1/2 that of proline.
  • 5.5. The pH optimum for proline oxidation lies between 6.5 and 7.5 based on RCR and ADP/O and between 7.0 and 7.4 based on state 3 rates.
  • 6.6. KCl concentrations between 250 and 450 mM gave optimal values for the oxidation of proline based on RCR and state 3 rates.
  • 7.7. KCl concentration had little effect on ADP/O between 100 and 850 mM.
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7.
  • 1.1. Studies were conducted in order to determine the combined effects of low environmental pH and temperature on embryonic survival capacity and metabolic rates in the dragonfly, Anax junius Drury. Studies were also conducted to assess the effects of hypoxia on hatching success as well as to investigate the role of hypoxia as a possible physiological triggering mechanism for hatching.
  • 2.2. At water temperatures of 10–30°C, an environmental pH value of 3.0 was extremely limiting and significantly reduced hatching success.
  • 3.3. Over a pH range of 3.0–5.0, a water temperature of 30°C was found to be severely limiting. Over a pH range of 6.0–7.0, hatching success was greater than 80% at test temperatures ranging from 10 to 25°C.
  • 4.4. Embryos of A. junius exhibited a greater tolerance to markedly low environmental pH (3.0) than that previously reported for fish and amphibians, although survival capacity was less than 10%.
  • 5.5. An environmental pH value of 3.0 has a significant detrimental effect on embryonic development. Survivorship and developmental rate increase significantly over a pH range of 4.0–5.0.
  • 6.6. Oxygen consumption rates were lowest for fertilized eggs exposed to a pH of 3.0 at all test temperatures (10–30°C). Metabolic rates increased significantly at pH 4.O.
  • 7.7. Embryos hatch successfully under hypoxic conditions in both aqueous and nonaqueous media. Results suggest that hypoxia acts as a triggering mechanism for hatching in this aquatic insect.
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8.
  • 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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9.
  • 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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10.
  • 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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11.
  • 1.1. Osmotic measurements were made on the perivisceral coelomic and water vascular fluids of 4 species of northwest Pacific starfish and their stable sea-water media.
  • 2.2. Mean levels of both fluids were hyperosmotic in every species, often at statistically significant levels.
  • 3.3. For all species combined, mean hyperosmolality (mosmol/kg ± SE) of perivisceral coelomic fluid was 1.49 ± 0.17, and water vascular fluid 6.07 ± 0.74.
  • 4.4. The hyperosmotic nature of these fluids contributes to water balance, working in conjunction with madreporitic inflow and other factors.
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12.
  • 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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13.
  • 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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14.
  • 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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15.
  • 1.1. The total body water, lipid content, and cuticular permeability of fungus infected and uninfected German cockroaches, Blattella germanica, were examined.
  • 2.2. Infected adult cockroaches weighed less and had significantly more body water than did uninfected specimens of the same size.
  • 3.3. Uninfected medium-size nymphs weighed significantly more than infected nymphs, but there was no difference in body size between infected and uninfected small nymphs.
  • 4.4. Cuticular permeability and lipid content of infected and uninfected cockroaches was not significantly different.
  • 5.5. Sequestering of water by the fungal cells is discussed as a possible factor in the pathology of this fungal parasite.
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16.
  • 1.1. The effect of regular handling on fear reactions was investigated in mallard (Anas platyrhynchos) by exposing six hand-reared and four wild ducks to an approaching human being and recording heart rates with an external ECG device.
  • 2.2. All ducks reacted to the approach with tachycardia, but the response was significantly less in tame birds.
  • 3.3. Hand-reared females showed less response than males. No sex-linked differences were apparent in the wild ducks.
  • 4.4. Decreasing responses throughout the experiments were only found in tame birds.
  • 5.5. Fear or stress reactions can apparently be diminished through habituation induced by regular handling.
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17.
  • 1.1. Total body water volume (TBWV) and daily water turnover rates (WTR) were measured in nestling and adult zebra finches using tritiated water (TOH).
  • 2.2. TBWV and daily WTR increased with age up to 13 days post hatching.
  • 3.3. TBWV and WTR approached adult levels after 13 days of age. WTR varied among ages and nest mates. All nestlings turned over at least 50% of their body water pool per day.
  • 4.4. The WTR data for adult birds are consistent with natural history data suggesting zebra finches are dependent on water for breeding and survival.
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18.
  • 1.1. Oxygen consumption and nitrogen excretion rates of Macrobrachium rosenbergii were recorded in media of varying salinities and ion compositions (Mevo Hamma, Yahel, Elat—continental water; and 15 and 24%. seawater dilutions).
  • 2.2. Oxygen consumption rates were not significantly different (P > 0.05) with the exclusion of Yahel having a metabolic rate of 0.258ml O2/gfw/hr which was significantly different from the other experimental media at the P ≲- 0.05 level.
  • 3.3. Nitrogen excretion rates were lowest in prawns adapted to Yahel water, 0.0188mg NH4-N/gfw/hr and increased with salinity to 0.0494mg NH4-N/gfw/hr in 24%.
  • 4.4. The O: N ratios ranged from 12.24 to 22.65 indicating that in dilute media (Mevo Hamma and Yahel) relative to saline media (15%, Elat and 24%) more lipids and carbohydrates are utilized as an energy substrate while the latter group increased protein catabolism.
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19.
  • 1.1. Accumulation and excretion of propionate and acetate during experimental anaerobiosis were investigated in the lugworm Arenicola marina.
  • 2.2. The rate of accumulation and the ratio propionate/acetate were found to be tissue-specific.
  • 3.3. The excretion of the volatile fatty acids showed a characteristic time course.
  • 4.4. The results of experiments analyzing the role of different organs indicate that the excretion of these metabolites proceeded via the undifferentiated surface of the body.
  • 5.5. The rate of excretion depended on the concentration gradient between animal and the ambient water, the chain-length of the fatty acid and the pH of the water. Propionate excretion was inhibited by butyrate.
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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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