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1.
  • 1.1. The effect of myo-inositol on the ability of three species of nematodes to survive desiccation has been studied.
  • 2.2. Survival rates obtained from worms treated with an inositol bathing medium were compared with survival rates of worms treated with distilled or tapwater media.
  • 3.3. Highest survival rates were found in those nematodes that were placed in an inositol solution prior to desiccation.
  • 4.4. Tapwater facilitated higher revival rates than did distilled water in both D. dipsaci and D. myceliophagous.
  • 5.5. No such differences were found for A. tritici.
  • 6.6. The results are discussed in relation to the possible mechanisms of protection afforded by the different bathing media.
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2.
  • 1.1. Eight ornate box turtles, Terrapene ornata, were heated and cooled in water at 35 and 15°C respectively.
  • 2.2. Thermal time constants were calculated and no significant differences were found (t-test; 0.05 level) between warming and cooling rates.
  • 3.3. Heart-rate data indicated slightly higher, but non-significant, mean values during warming.
  • 4.4. It was concluded that T. ornata is not able to physiologically alter rates of heat exchange in water significantly and must rely on behavioral mechanisms to maintain body temperature.
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3.
  • 1.1. The response to light of Hermissenda photoreceptors when recorded intracellularly without interference from synaptic and action potentials consisted of three phases: an early depolarization (ED) followed by hyperpolarization (dip) and subsequent depolarization (tail).
  • 2.2. The ED and the dip were associated with increased membrane conductance while decreased membrane conductance was involved with the tail.
  • 3.3. The dip reversal potential was − 82.1 ± 5.3 mV and its amplitude varied inversely with the log of [K+].
  • 4.4. Perfusing with agents which block K+ current like 4AP, Quinine, Quinidine or injection of TEA eliminated the dip and its associated increased membrane conductance, thus further supporting the role of K+ conductance in producing the dip.
  • 5.5. The dip was enhanced by increased [Ca2+]o, reduced by decreased [Ca2+]o and abolished together with its associated increased membrane conductance when perfused with either D600, Cd2+, Mg2+, Mn2+, or Co2+, which block transmembrane Ca2+ current.
  • 6.6. The dip and its associated increased membrane conductance were abolished by intracellular injection of EGTA and enhanced by perfusion with Ruthenium red.
  • 7.7. Intracellular injection of Ca2+ mimicked the dip: membrane conductance was increased and the cell hyperpolarized.
  • 8.8. These results indicate that the increase in intracellular [Ca2+] is primarily responsible for the light-induced increase of K+ conductance during the dip. The possible source of the Ca2+ is, at least in part, extracellular due to activation of an inward Ca2+ current.
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4.
  • 1.1. Chemical structures were determined for the cuticular alkanes, alkenes, and certain of the alkadienes for 11 D. virilis group species.
  • 2.2. Male-specific hydrocarbons occurred in five species: these were 9-heneicosene in D. americana and D. novamexicana, 10-heneicosene in D. virilis, 5,13- and 5,15-pentacosadienes in D. kanekoi, and 9-pentacosene in one strain of D. lummei.
  • 3.3. Hydrocarbon profiles of newly emerged flies always differed from mature files.
  • 4.4. Relationships among the species, with respect to hydrocarbon profiles, were investigated by cluster analysis.
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5.
  • 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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6.
  • 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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7.
  • 1.1. Patterns of osmoregulation were studied in three species of Swan river atherinids (Leptatherina presbyteroides, lower estuarine and marine; Craterocephalus mugiloides, mid estuarine; Leptatherina wallacei, upper estuarine) over a wide range of salinities.
  • 2.2. The plasma Na+ concentration was elevated with an increase in salinity.
  • 3.3. Haematocrit and body water content decreased with acclimation to higher salinity.
  • 4.4. All three species of atherinids osmotically regulated over a salinity range greater than that which these fish are reported to occur in.
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8.
  • 1.1. Intracellular recordings were made from the Retzius cells in the segmental ganglia of the leech, Hirudo medicinalis. L-Glutamate has a direct excitatory action on the neurons.
  • 2.2. L-Glutamate causes an increase in the membrane conductance.
  • 3.3. L-Glutamate causes conductance increase at the Retzius cell to both sodium and potassium ions but not to chloride ions.
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9.
  • 1.1. Rates of evaporative water loss (EWL) were measured in Anolis roquet and A. marmoratus each from three localities which varied in conditions of aridity.
  • 2.2. There were significant interpopulational differences in rates of EWL for both species which correlated with habitat aridity.
  • 3.3. Rates of EWL were significantly lower in A. roquet after 6 weeks acclimation to more xeric conditions, populational differences were still evident.
  • 4.4. Acclimational effects on rates of EWL were 2 to 3 times greater than populational differences.
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10.
  • 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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11.
  • 1.1. Filtering rates and oxygen consumption were measured in the field on a wild population of the fresh-water limnetic cladoceran Daphnia ambigua.
  • 2.2. Filtering rates increased with increasing body size and were significantly affected by environmental temperature.
  • 3.3. Oxygen consumption increased with increasing body size; there was no significant difference among b values determined at different environmental temperatures but bs were highest at low temperatures. decreased progressively at higher temperatures and increased at the highest temperatures.
  • 4.4. Temperature significantly affected the rate of oxygen consumption.
  • 5.5. Both filtering rates and oxygen consumption evidenced classical translation to the left in cold-acclimatized animals. An environmental temperature near 12°C apparently separates warm- and cold-acclimatization processes.
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12.
ab]
  • 1.1. Fennecs show marked diurnal variations of body temperature and heart rate.
  • 2.2. Basal metabolic rate (0.358 ml/ghr) is 39% lower than predicted by body mass, minimal conductance is reduced for 23%.
  • 3.3. Fennecs have a wide thermoneutral zone (23.4–32.0°C) and a low rate of evaporative water loss.
  • 4.4. Basal heart rate is considerably reduced. Oxygen pulse increases with decreasing ambient temperature. The higher oxygen demands below thermal neutrality, however, are met primarily by a rise in heart rate.
  • 5.5. Newborn fennecs show a metabolic response to cold from the first day of life.
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13.
  • 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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14.
  • 1.1. Studies characterizing glucose transport in the frog sartorius were performed.
  • 2.2. For nonstimulated and stimulated muscles, intracellular 2-deoxyglucose exceeded 2-deoxyglucose-6-phosphate at 15 min, showed little further increase, and was maintained below the extracellular concentration for 2 hr.
  • 3.3. Accumulated 2-deoxyglucose-6-phosphate did not inhibit glucose transport.
  • 4.4. Unlike in adipocytes, basal and stimulated 2-deoxyglucose transport showed no difference in sensitivity to N-carbobenzoxy-glycyl-l-phenylalaninamide.
  • 5.5. Phenylarsine oxide blocked contraction-enhanced 2-deoxyglucose uptake.
  • 6.6. These results suggest that the glucose transporter of the sartorius exhibits auto-regulation, and that basal transport is not regulated by the same process as in adipocytes.
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15.
  • 1.1. Freshwater gammarids from 900–1400 m depths lose Na at 1 atm, 4°C, while related shallow water gammarids are near neutral Na balance.
  • 2.2. Na+ influx rates are similar at 1 atm, 4°C, for abyssal and shallow water gammarids of similar weight.
  • 3.3. Na+ efflux is faster for abyssal gammarids than for comparable shallow water gammarids.
  • 4.4. Compressing abyssal gammarids to 90–140 atm increases Na+ influx rates enough to restore neutral Na balance, while in shallow water crustaceans, compression decreases Na+ influx.
  • 5.5. Na+ influx rates in Baikalian gammarids vary with the 0.55 power of weight.
  • 6.6. The equation Fma × t = 1.3 × W0.55 μEq/hr/animal applies to freshwater crustaceans over the weight range from 0.03 to 35 g.
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16.
Absract
  • 1.1. The basal metabolism of the vole, Microtus ochrogaster, a non-hibernator is about 80% below that expected for microtine rodents, while the basal metabolism of the chipmunk, Tamias striatus, is about 20% below that expected for small mammals.
  • 2.2. Blocking thyroid secretion results in a 3°C improvement in the vole. and a 2°C improvement in the chipmunk, to the highest air temperature tolerated.
  • 3.3. Blood levels of thyroxine in both species did not change as a function of ambient temperatures, whereas rates of radioiodine release were reciprocally related to ambient temperature.
  • 4.4. There was no indication that the thyroid gland of the chipmunk was ever inactive either preceding, or during, hibernation.
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17.
  • 1.1. The planktonic diatom Ditylum brightwellii, grown in light-limited resp. nitrogen-limited continuous culture, has been exposed to Cu levels, comparable with those in the Scheldt estuary.
  • 2.2. At increasing levels D. brightwellii initially detoxified Cu, producing metal-binding ligands (amino acids), and increasing its cell volume.
  • 3.3. In light-limited D. brightwellii, photosynthesis could be adjusted to increasing Cu stress, division rates remained constant, and cells proved to be adaptable to 200 nM dissolved Cu.
  • 4.4. Nitrogen-limited D. brightwellii detoxified Cu inadequately: it stored large amounts of Cu (30–60 μM) that inhibited cell division.
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18.
  • 1.1. Per cent total body water content (%TBW), cuticular permeability (CP), rate of water loss, critical thermal maxima (CTMax), and upper lethal limits (ULL) were determined for Pacific beetle, Diploptera punctata (Eschscholtz), Surinam, Pycnoscelus surinamensis (L.), and Turkestan, Blaita lateralis (Walker), cockroaches.
  • 2.2. Initial body mass ranged from 153.16 to 464.96 mg, for D. punctata and P. surinamensis cockroaches, respectively. Mean %TBW was 57.8 for P. surinamensis and 67.7 for B. lateralis.
  • 3.3. Mean cuticular permeability was not related to initial mass and ranged from 20.9 to 38.7 μg/cm2/hr/mmHg for D. punctata and P. surinamensis, respectively.
  • 4.4. Cumulative mass loss and %TBW lost increased linearly with desiccation time.
  • 5.5. CTMax ranged from 43.2°C for D. punctata to 44.3°C for P. surinamensis. There were significant, but small differences in CTMax among the three species.
  • 6.6. ULL were 2.2 to approximately 4°C greater than CTMax. The greatest ULL was 48.1°C for B. lateralis and the lowest ULL was 45.0°C for D. punctata.
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19.
  • 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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20.
  • 1.1. A comparison of proteolytic and protease inhibitory activity, and ecdysteroid levels in body fluids was made between normal larvae of the flesh fly, Sarcophaga bullata, and those that had been water-stressed for two days.
  • 2.2. The course of proteolytic activity in water stressed flies decreases 6 hr after beginning the experiment and remains low in comparison with control flies.
  • 3.3. The course of protease inhibitors exhibits a mirror image pattern to proteases.
  • 4.4. Ecdysteroid pattern shows two peaks in control animals: minor at 24 hr and major at pupariation, in experimental animals: at 1 hr, at 6 hr and at white pupal stage.
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