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1.
  • 1.1. The objective of the present work was to study the ontogeny of the ERG circadian rhythm in crayfish.
  • 2.2. Long-term recordings of ERG and shielding retinal pigments position measured from the instar, the second instar, the third instar and the adult crayfish were obtained.
  • 3.3. In the youngest animals (1–8 days old) an ultradian rhythm (15min-4hr periods) in the ERG amplitude was detected.
  • 4.4. Older animals showed a progressive increment in the period length before they exhibited a circadian pattern. This last appeared, the first time, in 30-day-old animals and showed noticeable differences in the adult crayfish. At the same time, the crayfish began to show photomotor reflex. Later on (140-day-old crayfish) the circadian rhythm attained its final parameters.
  • 5.5. The SD was used as a measure of lability in periods. The 4 hr ultradian rhythm and the 22.4 hr circadian rhythm showed the lowest SD indicating that they are the most precise period values.
  • 6.6. Our results support the idea that the ERG circadian rhythm results from the coupling among high frequency (ultradian) oscillators, particularly those of 4 hr periods and that the coupling depends on the action of neurosecretions released from the sinus gland.
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2.
  • 1.1. The oxygen consumption of the marine teleost, Lichia amia was investigated under controlled laboratory conditions.
  • 2.2. The routine oxygen consumption showed a strong circadian rhythm with the fish being mainly active during the light period.
  • 3.3. The specific mass exponent (dimension: μg O2/g/hr) is temperature independent and ranges from 0.27–0.29.
  • 4.4. Starving the fish results in a mean decrease in active, routine and standard oxygen consumption of 21%, 24% and 20%, respectively.
  • 5.5. Feecling led to an increase in the oxygen consumption of the teleosts, with the mean metabolic rate over the 24 hr that followed, being 58% and 50% higher for fish that had been starved for 162hr and 40 hr, respectively.
  • 6.6. Apparent SDA showed some variation and ranged from 6.0 to 35.5%.
  • 7.7. The results obtained are generally in agreement with those recorded for other teleosts.
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3.
  • 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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4.
  • 1.1. Using SDS-PAGE and immunoblotting analyses with anti-sorbitol dehydeogenase (EC 1.1.1.14, SDH) serum, changes in amount of SDH protein were examined in diapause and non-diapause eggs of the silkworm, Bombyx mori.
  • 2.2. When diapause eggs were exposed to 5°C from 2 days after oviposition to break the diapause gradually, SDH protein appeared after 50-day chilling, and then the amount increased along with chilling period. This changing pattern paralleled that in SDH activity.
  • 3.3. In diapause eggs treated with HCl after chilling at 5°C for 30 days to break the diapause quickly, and non-diapause eggs, changing patterns in amount of SDH protein also paralleled those in SDH activity.
  • 4.4. These results showed that SDH activity was caused by biosynthesis of SDH protein, independent of diapause or non-diapause eggs.
  • 5.5. Occurrence of SDH correlates with the three developmental phases: diapause termination, embryonic growth, and larval differentiation. In larva, SDH was mainly localized in the fat-body.
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5.
  • 1.1. Respiration rates of starved periwinkles, Liltorina littorea and Littorina obtusata, increased by 40–60% when fed their preferred algal food for 1 hr, or after having been exposed for the same period to an aqueous extract of the alga.
  • 2.2. The stimulus causing the rise in metabolic rate by algal extracts is therefore thought to be chemosensory in nature, and possibly composed primarily of dissolved free amino acids.
  • 3.3. The respiration rates of L. littorea responded only to the green alga Enteromorpha intestinalis while L. obtusata demonstrated an increase in respiration rates when fed the ubiquitous brown alga, Ascophyllum nodosum, and to a lesser degree to Enteromorpha.
  • 4.4. These results compare very well to postprandial increases in oxygen consumption demonstrated in vertebrates and marine bivalves where the components of specific dynamic action (SDA) are thought to be chiefly biosynthetic costs of digestion and assimilation.
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6.
  • 1.1. Some effects of restricting feed intake for 96 or 168 hr were determined in male Nubian goats.
  • 2.2. Goats restricted for 96 hr lost 11.6% of their body weight, and goats restricted for 168 hr lost 19.8%.
  • 3.3. Feed restriction for up to 168 hr did not produce significant effects on the heart rate, respiratory rate or rectal temperature.
  • 4.4. Haemoglobin concentration, packed cell volume and erythrocyte number were all decreased by feed restriction. There was also a tendency towards eosinopenia and lymphopenia.
  • 5.5. Feed restriction for 96 or 168 hr raised the plasma activity of aspartate transaminase, and did not affect significantly cholinesterase activity. Plasma amine oxidase activity was significantly reduced in goats restricted for 168 hr.
  • 6.6. Feed restriction produced significant increases in the blood or plasma concentrations of lactate. pyruvate, non-esterified fatty acids, cholesterol, ketone bodies and bilirubin.
  • 7.7. Significant decreases were found in the concentrations of total protein and calcium.
  • 8.8. No significant changes were observed in the plasma concentrations of glucose, sodium or potassium.
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7.
  • 1.1. Recordings were made from primary afferent and secondary neurons in the electrosensory system of the thornback ray.
  • 2.2. The frequency response characteristics of these neurons were determined during sinusoidal modulation of uniform external fields.
  • 3.3. The form or the filter curves was similar in all primary and secondary cells, with a maximum amplitude of response occurring at a modulation frequency of 4 Hz.
  • 4.4. Secondary neurons showed an increased gain at low stimulus amplitude, and saturated at a much lower level than primary afferents.
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8.
  • 1.1. Goldfish (Carassius auratus) were fitted with ECG electrodes and intra-cranial stainless steel electrodes to monitor cardiac, EEG and SPS responses, during minimal restraint, to presentation of environmental stimuli (light-on, moving shadow, tap).
  • 2.2. All three stimuli evoked a bradycardia and increases in the EEG frequency; correlates of arousal responses in fish.
  • 3.3. EEG frequency changes were most evident in the fore- and midbrain regions; in the hindbrain smaller responses nevertheless showed discrimination between stimuli.
  • 4.4. EEG amplitude changes were more site- and stimulus-specific than frequency changes.
  • 5.5. SPSs occurred on stimulus presentations which were negative in polarity in the midbrain and positive in the forebrain and hindbrain, though the latter were smaller and less consistent.
  • 6.6. Principal components analyses and regression analyses were used to examine detailed associations between peripheral and central physiological changes.
  • 7.7. It was found that increases in the EEG frequency of fore- and midbrain regions were related to cardiac deceleration on early stimulus presentations.
  • 8.8. This was also shown for the negative SPS of the midbrain to the presentation of the tap stimulus.
  • 9.9. Positive SPSs of the forebrain were related to the bradycardia on later stimulus presentation i.e. during habituation of the arousal response.
  • 10.10. The results indicate that in fish, as in other vertebrates, negative SPSs in the midbrain are associated with arousal and implicate the forebrain in the modulation of arousal by its habituation.
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9.
  • 1.1. Quick sinusoidal temperature fluctuations (constant average 10°C) cause an increase in metabolism in comparison to an invariable constant ambient temperature of the same dimension.
  • 2.2. At the observed mean value of 10°C metabolism is increased by 0.8% per 1 K/hr based on the values of resting metabolic rate (correlation: M = 53.5 + 0.445 Ta, M in J/K g hr, Ta = ambient temperature change in K/hr) and 0.6% based on the values of activity metabolism (M = 70.4 + 0.425 Ta).
  • 3.3. The absolute augmentation of metabolism per 1 K/hr is, by comparison, the same for day and night. Its amount is 0.42 and 0.43 J/K g hr respectively.
  • 4.4. In the response of metabolism to temperature fluctuations no differences could be found with respect to the amplitude and frequency modifications of temperature.
  • 5.5. The increase of energy consumption is probably caused to a greater extent by “overshoot” of the feedback control system in the course of adjusting metabolism to new levels according to the ambient temperature conditions.
  • 6.6. Short term ambient temperature changes (i.e. measuring different temperature levels in one night to test basic metabolism vs ambient temperature) cannot produce reasonable values for basic metabolic rate, since these artificially high values reflect the testing procedure.
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10.
  • 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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11.
  • 1.1. The activity of NAD-sorbitol dehydrogenase (NAD-SDH; EC 1.1.1.14) and levels of sorbitol were examined in non-diapause eggs of the silkworm, Bombyx mori, exposed to temperatures of 20-0.5°C from 1 day after oviposition. The morphology of embryos in the cold-acclimated eggs and the hatching of eggs after transfer to 25°C were monitored.
  • 2.2. Temperatures between 15 and 0.5°C retarded the development of NAD-SDH activity at a specific embryonic stage that was comparable to diapause, and sorbitol accumulated in the eggs.
  • 3.3. With the appearance of NAD-SDH activity, sorbitol was converted into glycogen, just as it is in diapause eggs. The results indicate that NAD-SDH participates in the utilization of sorbitol rather than in its formation in non-diapause eggs.
  • 4.4. Distinct effects of low temperatures on the morphological development of the embryos are also discussed.
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12.
  • 1.1.|The body temperature and activity of cats exhibit two-peak patterns during the 24 hr period.
  • 2.2.|The two peaks are retained when the temperature and activity are permitted to freerun.
  • 3.3.|A third prominent peak appears in the actograms in cats in the main colony, induced by the presence of humans.
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13.
  • 1.1. The mechanism of action of disulfiram on the respiratory electron transport system of the liver mitochondria was studied in vitro.
  • 2.2. Disulfiram inhibited the respiration supported by malate-glutamate as well as succinate.
  • 3.3. Mitochondrial respiration inhibition was dependent upon alteration of —SH groups.
  • 4.4. The inhibitory action of disulfiram might be related to the crosslinking of several proteins of the inner mitochondrial membrane.
  • 5.5. The effects described above could be attributed to disulfiram per se and not to the main metabolite diethyldithiocarbamate.
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14.
  • 1.1. Water vapour conductance (GH2O) was determined for 25 grey heron Ardea cinerea eggs in the laboratory, and in nests during natural incubation at two Scottish colonies.
  • 2.2. The mean GH2O of eggs measured in the nest which successfully hatched was 9.0 mgH;O/mmHg/day and the mean water vapour pressure gradient between egg and nest (ΔPH2O), measured using “calibrated” duck eggs, averaged at 31 mmHg (4.13 kPa).
  • 3.3. Based on eggshell porosity results, from the eggs which hatched, such a gradient would result in a loss of water from the eggs during incubation equivalent to 11% of their fresh weight.
  • 4.4. Shell thickness, the number of pores/cm2 of eggshell and DDE content were also determined for the 25 eggs measured in the laboratory.
  • 5.5. Eggs containing high levels of DDE had thinner shells, more pores in the eggshell and a higher overall eggshell porosity.
  • 6.6. The main problem posed by a high level of DDE would appear, however, not to be an excessive water loss from the egg during incubation, but rather eggshell thinning leading to a loss of the egg due to breakage in the nest.
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15.
  • 1.1. Eel were exposed to a sublethal concentration of lindane (0.335 ppm) for 6, 12, 24, 48, 72 and 96 hr.
  • 2.2. Concentrations of glycogen, glucose, lactate, pyruvate and lipids were determined in gill tissue after lindane exposure.
  • 3.3. Gill glycogen descreased and glucose levels increased at 6 hr of treatment, lactate and pyruvate concentration increased between 6 and 48 hr. Total lipid values decreased between 6 and 24 hr; thereafter, the levels increased up to 72 hr of exposure.
  • 4.4. Clear changes were found in all parameters tested in gill tissues. The observed effects of lindane on metabolism in fish are discussed in relation to acute stress syndrome.
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16.
  • 1.1. The light irradiation at examined wavelengths between 360 and 630 nm enhanced the respiratory rate in the presence of CO in sperm, as well as eggs, of the sea urchins, Anthocidaris crassispina and Hemicentrotus pulcherrimus, the starfish, Asterina pectinifera, and the echiuroid, Urechis unicinctus.
  • 2.2. The maximum peaks of stimulating effects of light irradiation on CO-insensitive respiration were found at wavelengths of 430, 530 and 570 nm in sperm of these species.
  • 3.3. The respiration in the presence of CO was insensitive to light irradiation in sperm and eggs of the oyster, Crassostrea gigas and the tunicate, Ciona intestinaris.
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17.
  • 1.1. The rate of oxygen consumption has been monitored continuously in M. edulis during acute exposure to high sublethal concentrations of formaldehyde, phenol and benzene and subsequent recovery periods of 96 hr.
  • 2.2. The results are discussed in relation to changes in the electrochemical potential difference of sodium, the content of ATP and the tissue concentration of strombine.
  • 3.3. After exposure to benzene and phenol, an increase in the rate of oxygen consumption that could not be explained by oxygen debt from the exposure period was observed.
  • 4.4. Depression of the rate of oxygen consumption after exposure to formaldehyde may be explained by a reduced ability to extract oxygen from the water.
  • 5.5. The pattern of oxygen consumption and behavioural responses, as well as the combined changes in the biochemical markers, were distinctly different in the three cases.
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18.
  • 1.1. Inorganic ion content of developing follicles and of whole eggs and separated embryos and yolk sacs of the viviparous lizard, Sphenomorphus quoyii has been measured.
  • 2.2. There is a net increase in calcium, sodium and potassium in whole eggs during gestation. Magnesium and phosphorus content remains constant.
  • 3.3. The additional ions are incorporated into the developing embryo.
  • 4.4. Calcium content of the yolk is compared with that of the fowl and other species of reptile.
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19.
  • 1.1. Renal function in migrating adult Atlantic salmon was studied in sea-water (SW) and following abrupt transfer to fresh water (FW).
  • 2.2. Urine flow rate of SW-adapted fish, 0.72 ml/kg/hr, increased 6.3-fold to 4.55 ml/kg/hr after 2–3 days in FW, later decreasing to around 1 ml/kg/hr.
  • 3.3. Changes in glomerular filtration rate and ion filtration rates largely paralleled changes in urine flow. In SW-adapted salmon about 4% of excreted magnesium is filtered. Tubular magnesium secretion declined within 1 day of FW transfer.
  • 4.4. During the period of maximum diuresis, urinary sodium loss is 77% of the branchial sodium uptake rate. This falls to less than 20% in FW-adapted fish.
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20.
  • 1.1. The influence of temperature (14,19, 24°C), salinity (26,32, 38,44%.) and food type (artificial diets: Fryfood, Mytilus, Soya, Yeast, Spirulina) on the respiratory rate of Tisbe holothuriae has been studied.
  • 2.2. Oxygen consumption decreased with decreasing temperature, but with a greater rate at supra- or subnormal salinities.
  • 3.3. Multiple-regression analysis showed the quadratic effect of temperature and the linear effect of salinity to be the more important factors affecting respiration.
  • 4.4. The food type also seems to exert an important effect on oxygen consumption.
  • 5.5. A significant lowering of respiration was observed for all food tested when the animals were starved.
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