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1.
  • 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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2.
  • 1.1. The effect of eyestalk ablation on preadults of Callinectes similis exposed to a constant salinity (30%.) and to simulated tidal changes in salinity (30-11 to 30%.) were measured.
  • 2.2. In constant salinity, crabs showed a persistent respiratory rhythm, with a maximum oxygen consumption during the day. Under these conditions, ablation significantly increased the respiratory rate but not the rhythm.
  • 3.3. In variable salinities, the highest respiratory rates occurred in salinities of 11 and 16%. during the night. In these crabs, ablation of eyestalks and subsequent injection of eyestalk extracts did not alter the respiration rate rhythm.
  • 4.4. The circadian rhythm is controlled by the periodicity of environmental changes instead of the influence of eyestalk hormones.
  • 5.5. Regulation of metabolism in C. similis associated with osmoregulation involves other neurosecretory organs.
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3.
  • 1.1. Chronic administration of melatonin (in silastic capsules) lengthened the free-running period of the locomotor rhythm and shortened the circadian activity time in Podarcis sicula held in constant temperature and darkness.
  • 2.2. Lizards displaying a bimodal pattern of activity invariably became unimodal after melatonin administration.
  • 3.3. The results support the hypothesis that melatonin acts as a coupling device between circadian oscillators driving the locomotor rhythm in Podarcis sicula.
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4.
  • 1.1. The adult possums showed a circadian rhythm of body temperature with a peak in temperature around midnight and a nadir at noon.
  • 2.2. The young possum within the pouch displayed a circadian rhythm with the highest temperatures during the day and the lowest in the early evening.
  • 3.3. Although the body temperature of the young possum exceeded that of the mother occasionally, for the major part of the 24 hr the body temperature of the young was lower than that of the mother.
  • 4.4. The young possum could maintain a steady body temperature between 140 and 167 days post partum. A circadian rhythm of temperature was observed between 157–190 days post partum.
  • 5.5. All adipose tissue examined with the light and electron microscope had the morphology of white adipose tissue.
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5.
  • 1.1. The procedure used to compare the forced running performance of three rodent species was the number of electrical stimuli required each minute to keep the animals running.
  • 2.2. During running trials, ground squirrels, Spermophilus tridecemlineatus, required fewer stimuli than white rats. Squirrels ran 12.4 ± 6.9 (2 SE) min before requiring stimulation vs 3.1 ± 1.4 min for rats.
  • 3.3. Total oxygen consumption during the running period was significantly higher for ground squirrels than white rats, 4.70 ± 0.36 and 4.18 ± 0.38ml O2/g/hr, respectively.
  • 4.4. Heart weight/body weight ratios were significantly higher for the ground squirrels than the white rats.
  • 5.5. No differences were noted between ground squirrels and chipmunks other than those which could be accounted for by body weight differences.
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6.
  • 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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7.
  • 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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8.
  • 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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9.
  • 1.1. It is shown that Ca2+-dependent activation of respiration of liver mitochondria from hibernating ground squirrels is accompanied by mitochondrial swelling.
  • 2.2. The swelling of mitochondria from hibernating ground squirrels, as well as the activation of mitochondrial respiration, is precluded by cyclosporin A, p-bromphenacylbromide and oligomycin. Carboxyatractiloside, on the contrary, under these conditions favors the swelling and the acceleration of respiration.
  • 3.3. It was concluded that Ca2+-dependent activation of hibernating ground squirrel liver mitochondrial respiration resulted from the appearance of a non-specific permeability pathway and from swelling of mitochondria.
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10.
  • 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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11.
  • 1.1. Developing eggs of whitefish (Coregonus lavaretus L.) and vendace (Coregonus albula L.) were kept at 1–2°C and some eggs taken gradually up to 8°C to provoke mass hatching of embryos.
  • 2.2. Wet weight, dry matter and the contents of lipid, protein and ash were measured in fish during the course of experiment.
  • 3.3. Dry matter content decreased gradually in whitefish eggs from 15.64 to 11.95% during 1 month at 1–2°C, whereas vendace eggs showed only a slight decrease from 16.27 to 15.53%.
  • 4.4. In both species protein content decreased but lipid increased when approaching the natural time of hatching.
  • 5.5. During delayed hatching at low water temperatures protein contributes to catabolism, whereas lipid content decreased only in the later phase of the experiment.
  • 6.6. Larvae starved for 10 days after hatching lost increasing amounts of dry matter (from 26.1 to 50.3% of body weight) and protein (from 18.7 to 45.9% of body weight) as they remained longer in cold water as embryos.
  • 7.7. A correspondence was found between assessment of metabolic utilization of body stores based on chemical analysis of fish body and previous work on oxygen consumption and nitrogen excretion.
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12.
  • 1.1. The weight and energy content of sloughed skins of 92 individual snakes of 22 different species in three families were measured.
  • 2.2. Weight and total energy content of shed skins were highly correlated with body weight.
  • 3.3. The heat of combustion (kJ/g) of sloughed skins varied significantly among families and was higher in species having unkeeled scales than in those with keeled scales.
  • 4.4. The presence of keels significantly affected weight of skins, even when skin weight is adjusted for covariance with body weight.
  • 5.5. Neither body weight nor ambient temperature significantly affected the heat of combustion of sloughed skins.
  • 6.6. The energy content of shed skin, expressed as a proportion of daily metabolism, decreased with ambient temperature, but the effect is minimized in large snakes.
  • 7.7. Small snakes expended relatively less energy in sloughed skins than large snakes when the expenditure is expressed in terms of total daily metabolized energy.
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13.
  • 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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14.
  • 1.1. Fundamental chitin digestion characteristics of Crassostrea virginica crystalline style were investigated.
  • 2.2. Optimum temperature and pH were 34°C and 4.8. respectively.
  • 3.3. The colloidal regenerated chitin (0.56mol/0.5 ml: GlcNAc equivalents) was saturating under all enzyme levels encountered.
  • 4.4. There was no evidence of end product inhibition, even after 100 hr incubation.
  • 5.5. Calculated Km for the chitinase complex was 1.19mM when determined using a 30 min assay, but was only 0.70 mM when determined using a 4.6 hr assay.
  • 6.6. Both Km values are lower than reported for similar assays in other molluscs and for most bacteria.
  • 7.7. Effect of substrate preparation on the kinetics are discussed.
  • 8.8. Eight peaks of chitinase activity were resolved by DEAE-Fractogel ion exchange chromatography.
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15.
  • 1.1. An examination of calcium homeostasis in a facultative hibernator, the golden hamster (Mesocricetus auratus) was made.
  • 2.2. Fresh bone length and weight, and ash bone calcium and phosphorus were examined in normo-thermic, cold-acclimated and hibernating hamsters.
  • 3.3. Although fresh bone weight changes were noted, when corrected for body weight, no change was seen in either hibernating or cold-acclimated animals. Bone calcium and phosphorus were similarly unaffected by these forcings.
  • 4.4. The data are supported by histologie studies of bone and constant plasma calcium values, and are discussed in terms of mechanisms underlying alterations in mineral balance.
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16.
  • 1.1. An elastase-like enzyme was purified from the pyloric caeca of rainbow trout by hydrophobic interaction, cation exchange and gel-filtration chromatography.
  • 2.2. The approximate molecular weight of the elastase was 27 kDa and the isoelectric point was remarkably basic.
  • 3.3. The pH optimum of this enzyme was 8.0, when assayed with Succinyl-Ala-Ala-Ala-p-Nitroanilide.
  • 4.4. When assayed with Succinyl-Ala-Ala-Ala-p-Nitroanilide, the enzyme activity had a temperature optimum of 45°C, and the enzyme was stable up to this temperature.
  • 5.5. The trout elastase exhibited a higher specific activity than porcine elastase against Succinyl-Ala-Ala-Ala-p-Nitroanilide and elastin-orcein.
  • 6.6. The trout elastase was inhibited by elastatinal, PMSF, TPCK, SBTI and Bowman-Birk inhibitor.
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17.
  • 1.1. Size and composition of sagittal otoliths from red drum, Sciaenops ocellatus (Sciaenidae), reared at various constant temperatures were compared with otoliths from wild-caught fish.
  • 2.2. Uncoupling of otolith growth and somatic growth in laboratory-reared fish was evident in otolith length, area, volume, weight, density, and organic fraction.
  • 3.3. Fish grown at low temperatures had significantly smaller and less dense otoliths having a greater organic content than fish of the same size grown at higher temperatures.
  • 4.4. Changes in inorganic elements were poorly related to temperature in laboratory-reared fish.
  • 5.5. The effect of temperature on otolith elemental composition was small relative to the effects of age and its associated physiological changes.
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18.
  • 1.1. Changes in the glycogen content, condition, stomach content and acetic acid concentration of mussels Mytilus edulis and cockles Cerastoderma edule were followed during periods of up to 14 days of exposure (to air) at temperatures of 5 and 20°C.
  • 2.2. In animals with a high glycogen content the glycogen is not used during the first 3 to 7 days, at high and low temperature respectively.
  • 3.3. After this latent period the glycogen concentration often decreased, coinciding with a high mortality and an increase of the concentration of acetic acid.
  • 4.4. In cockles with a low glycogen content, and kept at a high temperature, glycogen can be used from the beginning of the stress period.
  • 5.5. Between species no clear differences were found.
  • 6.6. The stomach content decreased during exposure; however, the stomach content amounted to only 0.5 to 0.7% of the body weight, and is thought to be of minor importance as an energy source during the stress period.
  • 7.7. Especially at the higher temperatures glycogen finally is transformed into acetic acid.
  • 8.8. It is concluded that during exposure, the animals do not die because of a lack of energy reserves, but because of a high accumulation of acids.
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19.
  • 1.1. The copepod Tisbe holothuriae was collected from the Saronicos gulf of Greece and cultured in the laboratory, under dif'erent combinations of temperature and salinity and as well as different types of food.
  • 2.2. The content of C, H and N in females was measured.
  • 3.3. As temperature increases and salinity declines from 38%, the content of C, H and N per individual decreases.
  • 4.4. The type of food influences the carbon and hydrogen content per individual, while the nitrogen content is relatively constant.
  • 5.5. The percentage content of C, H and N in females without egg sacs and females carrying their first newly formed egg sacs do not differ significantly
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20.
  • 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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