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1.
  • 1.1. The concentrations of free glycerol, inositol and trehalose in five species of nematodes were determined. Analyses of total inositol content were also made.
  • 2.2. Significant differences in free and bound sugar levels were found between the two good anhydrobiotes Anguina tritici and Ditylenchus dipsaci and the three poor survivors Pangrellus redivivus, D. myceliophagous and Turbatrix aceti.
  • 3.3. Highest trehalose contents were found in desiccated A. tritici and D. dipsaci, but glycerol levels were low.
  • 4.4. P. redivivus and T. aceti contained high concentrations of free glycerol.
  • 5.5. Desiccated A. tritici larvae contained more free and bound inositol than all other species studied, but desiccated D. dipsaci larvae had higher levels of bound inositol than P. redivivus, D. myceliophagous and T. aceti.
  • 6.6. Dramatic reductions in inositol and trehalose contents were found in revived A. tritici larvae and freshly extracted D. dipsaci larvae. This was accompanied by an increase in glycerol content.
  • 7.7. The results are discussed in relation to the possible biochemical adaptations employed by anhydrobiotes during desiccation.
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2.
  • 1.1. Twenty organohalogen compounds, primarily phenols, were detected in the volatile extracts of the acorn worm Ptychodera bahamensis.
  • 2.2. Five chlorinated compounds, previously undescribed from acorn worms, were identified.
  • 3.3. Enteropneusts can be significant contributors of halogenated organics to the marine environment.
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3.
  • 1.1. Aspects of the physiology of two southern African scorpions have been examined. The scorpions are the large desert species Parabuthus villosus (Peters) (Buthidae) and the more mesic, burrowing species Opisthophthalmus capensis (Herbst) (Scorpionidae).
  • 2.2. Evaporative water losses were higher in Opisthophthalmus at all temperatures.
  • 3.3. Analysis of haemolymph during prolonged desiccation showed good osmotic and ionic regulation in Parabuthus but no regulation in Opisthophthalmus.
  • 4.4. Oxygen consumption of Parabuthus was measured after acclimation to 10 and 30°C. Metabolic rates were extremely low but there was no metabolic compensation to increased temperatures.
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4.
  • 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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5.
  • 1.1. Protein composition of different stages of Schistosoma mansoni was compared using specific antisera, 2D polyacrylamide gel electrophoresis and 14-C-leucine incorporation into proteins.
  • 2.2. Major qualitative differences were detected when an anti-membrane antiserum was used.
  • 3.3. 2D gel electrophoresis showed that the protein composition varied when mature and immature females were compared, whereas no differences were noted when mature and immature male worms were compared.
  • 4.4. Experiments measuring protein synthesis by the different schistosome stages confirmed that upon maturation, only the female schistosomes displayed qualitative differences.
  • 5.5. The protein pattern of the male schistosomes did not vary significantly as a function of development.
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6.
  • 1.1. Thymidine uptake kinetics in 10-day old crowded (100 worms/rat), 10 day uncrowded (10 worms/rat) and 6-day old H. diminuta were investigated. Succinate, a partial mediator of the “crowding effect” was also tested for its effect on the thymidine uptake of uncrowded worms.
  • 2.2. Immature (6-day old) H. diminuta have a high affinity transport site for thymidine which persists in the anterior regions of 10-day old worms, but is overshadowed by the proliferation of lower affinity sites in the remainder of the 10-day old strobila.
  • 3.3. Lower rates of 3H thymidine incorporation into DNA by crowded or succinate-treated worms cannot be accounted for by differences in thymidine uptake characteristics.
  • 4.4. The inclusion of 14C-PEG in uptake experiments as a non-absorbable marker is of particular use when studying small, young worms with high surface to mass ratios.
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7.
  • 1.1. At 37 stations in the English Channel and the southern North Sea concentrations of four brominated phenols in Lanice conchilega were determined using ECD equipped capillary gas chromatography: 2,4-dibromophenol, 2,6-dibromo-4-methylphenol, 2,4,6-tribromophenol, 3,5-dibromo-4-hydroxybenzaldehyde.
  • 2.2. Concentrations in worms of the southern North Sea were generally below 1 μg/g wet wt.
  • 3.3. Levels were slightly raised in worms of sheltered shores, those of 3,5-dibromo-4-hydroxybenzaldehyde were increased in subtidal populations.
  • 4.4. Concentrations in L. conchilega of Brittany were considerably higher than those in worms of the Frisian Islands, North Sea; they deviated from the latter by factors of 3, 16, 4, 4, respectively.
  • 5.5. The reasons for the conspicuous differences are hitherto unknown; three explanations are suggested.
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8.
  • 1.1. Drosophila mettleri have been found feeding but not breeding on decaying stems of senita cactus, the normal host for Drosophila pachea.
  • 2.2. Alkaloids were extracted from senita stems and used in tests of egg-to-adult viability, developmental rate, and adult longevity.
  • 3.3. The results show that developmental rate is not appreciably affected by senita alkaloids.
  • 4.4. In general, D. mettleri was less affected by the alkaloids with respect to egg-to-adult viability and adult longevity than D. pachea at concentrations which are fatal to other desert Drosophila.
  • 5.5. Tolerance to alkaloids gives D. mettleri an ecological advantage.
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9.
  • 1.1. Replacing chloride (Cl) with sulfate (SO42−) in the bathing medium drastically reduced the mucosal membrane potential difference (ψm).
  • 2.2. The voltage divider ratio was significantly greater than one.
  • 3.3. Mucosal d-glucose decreased the input resistance of the intestinal epithelium.
  • 4.4. Addition of furosemide to the mucosal bathing medium inhibited transepithelial potential difference and short-circuit current.
  • 5.5. Addition of SITS to the mucosal bathing medium partially inhibited transepithelial potential difference and short-circuit current.
  • 6.6. Diffusion potentials in the intestinal epithelium were symmetrical.
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10.
  • 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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11.
  • 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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12.
  • 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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13.
  • 1.1. The incorporation of myo-[2-3H]inositol into phosphatidylinositols was unmodified in brain cortex miniprisms from convulsant rats.
  • 2.2. However, the incorporation had increased by 300–400% in non convulsant rats which had received the same amount of lindane at a lower concentration.
  • 3.3. This result suggests that phosphatidylinositols are implicated in the convulsion syndrome.
  • 4.4. Experiments with lindane added in vitro were performed with both subchronically lindane intoxicated and untreated rats.
  • 5.5. The results show an interesting lack of parallelism.
  • 6.6. This might indicate the development of some resistance to the effects of lindane, possibly as the result of complex compensatory changes in inositol lipid biosynthesis.
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14.
  • 1.1. myo-Inositol concentrations in oviduct, ovary and uterus were many-fold those of blood serum during all four stages of the estrous cycle of the female rat.
  • 2.2. Inositol concentration was higher in oviduct than in ovary or uterus and was lower in uterine fluid than in uterus.
  • 3.3. Estrus uteri had higher inositol concentrations than uteri in other phases of the cycle.
  • 4.4. In order to measure dynamic aspects of the distribution of inositol. the distribution of radioactivity among organs of the reproductive tract of mature female rats was measured 45 min after i.p, injection of [2-3H]myo-inositol.
  • 5.5. These organs concentrated inositol from the blood, and the tissue radioactivity (expressed as dpm/mg wet wt of tissue) increased in the sequence: vagina < cervix < uterus < ovary < oviduct.
  • 6.6. The uterus and ovary concentrated myo-inositol more strongly during proestrus than during metestrus. diestrus or estrus.
  • 7.7. The contents of proestrus follicles were more highly radioactive than was the ovary itself, whereas proestrus uterine fluid was less radioactive than the uterine tissue.
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15.
  • 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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16.
  • 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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17.
  • 1.1. In late winter, oxygen consumption of honey bee (Apis mellifera L.) clusters showed marked 24-hr periodicity, even when held under constant temperature conditions.
  • 2.2. Minimal rates of metabolism (as low as 3.4 w kg −1) were usually reached at night (ca. 0500 hr), and maximum rates (as high as 33.5 w kg−1) in midday (ca. 1400 hr).
  • 3.3. Colonies with brood showed less excursion in daily metabolic rate, by maintaining higher night-time levels.
  • 4.4. There is a pronounced decrease in metabolic rate for the intact cluster of 9480–23,394 bees from the rates reported for individuals or small groups of bees.
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18.
  • 1.1. Mortality was 100% at pH 3.5 over a temperature range of 10–30°C for embryos and nymphs of Caenis diminuta and C. hilaris.
  • 2.2. Hatching success for both species was highest at pH values above 4.5.
  • 3.3. Survival capacities were significantly higher at 20°C over a pH range of 4.0-7.2.
  • 4.4. Oxygen consumption rates increase as a function of increasing temperature and reduced acidity.
  • 5.5. Loss of the nymphal righting response was observed at pH 3.5. This response can be used as a behavioral assay for acid stress.
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19.
  • 1.1. The relationship between host and parasite rates of energy metabolism was used to estimate the energy burden of Argeia pauperata on its host Crangon franciscorum.
  • 2.2. Respiration rates of the host were not significantly affected by the parasite even though the caloric turnover rate of the parasite was more than three times that of the host.
  • 3.3. The ratios of both energy expenditure and size of the parasite to those of the host were positively correlated with host size.
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20.
  • 1.1. An alkaline p-nitrophenylphosphate phosphatase has been purified 440-fold from extracts of Hatobacterium halobium.
  • 2.2. The enzyme has an apparent molecular weight of 24,000.
  • 3.3. A Km value for p-nitrophenylphosphate of 1.12mM has been found under optimal conditions.
  • 4.4. The enzyme is selectively activated and stabilized by Mn2+.
  • 5.5. It requires high salt concentrations for stability and maximum activity.
  • 6.6. It displays an unusual restricted substrate specificity of 25 phosphate esters tested, only phosphotyrosine and casein were hydrolysed besides p-nitrophenylphosphate.
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