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1.
  • 1.1. Anterior byssus retractor muscle of Mytilus (ABRM) was stimulated to contract by ACh (acetylcholine) and effects of temperature (5–30°C), FDNB (1-fluoro 2,4 dinitro-benzene) and IAA (iodoacetic acid) on tension response were examined.
  • 2.2. Isometric tension was highest at the temperature range of 10–20°C and decreased at higher and lower temperature than that range.
  • 3.3. The rate of tension decay after washing of ACh was accelerated by the increase of temperature.
  • 4.4. Tension redevelopment after release of 1 % during contraction was much smaller at 5°C than at 20°C.
  • 5.5. Tension development by ACh and the rate of tension decay after washing of ACh were remarkably decreased by the treatment of FDNB or IAA.
  • 6.6. The above results were discussed from the viewpoint that energy metabolism might be related to catch.
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2.
  • 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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3.
  • 1.1. The cardiovascular physiology of adult Carcinus maenas (L.) emerging into air has been investigated at three different air temperatures.
  • 2.2. Transition from seawater to air or vice versa triggered transient increases in cardiac and locomotor activity.
  • 3.3. However, crabs became inactive 5–10 min after emerging from seawater (15°C) into air at the same temperature (15°C) or at lower temperatures (12–13°C) and heart rate fell.
  • 4.4. At higher air temperatures (18–20°C) heart rate rose but to a lesser extent than predicted from aquatic Q10 heart-rate values.
  • 5.5. Crabs were again quiescent in aerial conditions.
  • 6.6. Mean arterial oxygen tension (Pao2) was ~ 74 mmHg in submerged crabs but fell to ~ 38 mmHg in air while mean arterial carbon dioxide tension (Pao2) increased from 1 to 4 mmHg resulting in respiratory acidosis.
  • 7.7. A model of gill function is proposed to explain the development of internal hypoxia in air.
  • 8.8. The results are discussed in relation to the distribution of adult and juvenile C. maenas in situ.
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4.
  • 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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5.
  • 1.1. The temperature and water relations of Centruroides hentzi females were investigated. At 12 and 72% relative humidity (RH), the lower and upper Lt50 were -4.5 and 43.7°C, and -4.7 and 45.1°C, respectively. When exposed to high temperature stress, survivorship was significantly greater under mesic conditions.
  • 2.2. Cuticular water loss was higher under xeric conditions (12% RH), ranging from 0.061 mg/cm2/hr at 30°C to 0.211 at 41°C.
  • 3.3. Exposure to dry air (0–5% RH) resulted in a significant increase in hemolymph osmolality: from 441 to 688 mOsm over a 5 day period.
  • 4.4. Mean oxygen consumption rates increased from 161.7 mm3/g/hr at 34°C to 541.6 at 44°C. ATPase activity was significantly higher in animals acclimated and tested at 35°C.
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6.
  • 1.1. Proteolytic, lipolytic, amylolytic and cellulolytic activities were studied in adults of the phytophagous beetle, Hydromedion sparsutum, indigenous to the sub-Antarctic island of South Georgia.
  • 2.2. Gastric enzyme activities were measured at experimental temperatures of 5–40°C and results were compared with those obtained from two thermophilic insects, Gryllus bimaculatus and Tenebrio molitor.
  • 3.3. Protease and lipase activities in Hydromedion were 10–15 times lower than in Gryllus and Tenebrio.
  • 4.4. In the temperature range of 5–15°C, α-amylase activity from Hydromedion was only slightly lower than that from Gryllus.
  • 5.5. Hydromedion gut homogenates exhibited a distinct cellulolytic activity, even at a low temperature of 5°C.
  • 6.6. Cellulolytic activity in the digestive tract of Hydromedion was confirmed by the evolution of 14CO2 after consumption of labelled cellulose.
  • 7.7. The thermal properties of digestive enzymes agree well with the role of Hydromedion as primary decomposer in its ecosystem.
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7.
  • 1.1. A lipoxygenase activity was purified from Thermoactinomyces vulgaris and some of its properties were characterized.
  • 2.2. The enzyme showed a temperature activity range of 40–55°C with still significant activity over 60°C.
  • 3.3. The pH of activity on linoleic acid had a broad range with an optimum at pH 6.0 and a weaker one at pH 11.0.
  • 4.4. On arachidonic acid the pattern was narrow bell-shaped with an optimum at pH 6.5.
  • 5.5. The purified lipoxygenase from Th. vulgaris showed an apparent Km of 1 mM and Vmax of 0.84 μmol diene/min/mg protein.
  • 6.6. It was inhibited by the oxidation products, 9-HPOD and 13-HPOD.
  • 7.7. A 160,000 Da molecular weight of the enzyme was determined by molecular filtration. Methionine, tyrosine, tryptophan and cysteine are apparently involved in its activity.
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8.
  • 1.1. G3PDH was isolated from the lateral muscle of rainbow trout (Salmo gairdneri) acclimated at 5°C (cold) and 15°C (warm).
  • 2.2. No differences were found in muscle concentration, molecular weights, isoelectric focusing patterns, amino acid compositions or peptide maps between cold and warm isolates.
  • 3.3. Cold and warm G3PDH contained mannose in variable concentration but no other prosthetic groups.
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9.
  • 1.1. Common carp (Cyprinus carpio) exposed to experimental temperatures of 12, 18, 24, 30 or 36°C for a 4-week period were used to investigate the effect of temperature acclimation on the frequency of opercular movement (FOM), growth and cytochrome c oxidase (CCO) activity in heart, liver and muscle.
  • 2.2. An exponential relationship between FOM and temperature after the first week (1010 =1.76) disappeared after the second week.
  • 3.3. The initially high FOM at temperatures of 30 or 36°C and the low FOM at 18 or 12°C changed over 4 weeks to approach the FOM of fish at 24°C.
  • 4.4. This change in the relationship of FOM to temperature from highly dependent to independent appeared to be thermal compensation.
  • 5.5. Heart and liver CCO activities were significantly affected by temperature, with the lowest activity at the approximate optimum temperature for growth, 24°C.
  • 6.6. Highest CCO activities for heart and liver occurred at both the highest and lowest temperatures.
  • 7.7. Among the three tissues, heart CCO activity was generally the highest and most affected by acclimation temperature.
  • 8.8. Muscle tissue had the lowest CCO activity and was unaffected by temperature.
  • 9.9. The high CCO activity at a cold acclimation of temperature 12°C was probably due to thermal compensation and the high activity at 36°C may have been a result of thermal stress.
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10.
  • 1.1. Cardiac frequency patterns of Callincctes sapidus Rathbun were used to evaluate potential thermal stress after exposure to 5°C increases over a range of acclimation temperatures from 5° to 30°C.
  • 2.2. An acclimated rate-temperature curve (R-T curve), acute R-T curves of the stabilized rates at the increased temperatures and Q10 temperature coefficients were used to assess the significance of the changes in rate frequency.
  • 3.3. The acclimated R-T curve showed that blue crabs go through a series of seasonal adaptation types characterized by a plateau of perfect adaptation for both cold and warm adapted organisms. Paradoxical adaptation occurred between the transition from cold to warm acclimation temperatures.
  • 4.4. The acute R-T curves showed that cardiac frequency was highly responsive to a 5°C increase when the organisms were acclimated to low temperatures.
  • 5.5. The Q10's of the acute R-T curves at the warm acclimation temperatures approximated those values derived for the acclimated R-T curve.
  • 6.6. This suggests that the temperature increase had a negligible effect on the warm adapted crabs, that is, little or no thermal stress occurred.
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11.
  • (1)We designed a physical model that simulates the thermal and evaporative properties of live Western toads (Bufo boreas).
  • (2)In controlled tests, the model tracked the body temperature of live toads with an average error of 0.3±0.03 °C (test range=4–30 °C).
  • (3)It estimated the evaporative water loss of live toads with an average error of 0.35–0.65  g/h, or about 14% (test range=0.7–9 g/h).
  • (4)Data collected with this physical model should provide an effective way for biologists to better understand habitat selection in toads and other amphibians
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12.
  • 1.1. The ambient temperature of embryos of pipped eggs was reduced from 38 to 28°C for a period of 45 min.
  • 2.2. The blood PCO2 was lower and the blood more alkaline at 28°C than at 38°C.
  • 3.3. At 28°C plasma [HCO3] ] was lower than predicted from the blood buffer line determined in vitro.
  • 4.4. The plasma concentrations of strong ions and lactate were the same at both temperatures.
  • 5.5. After the ambient temperature had been returned to 38°C for a period of 45 min, blood pH was more acidic than before cooling, but there was no difference in blood PCO2.
  • 6.6. The plasma [HCO3] was the same as that at 28°C and plasma [K+] was higher than before cooling.
  • 7.7. The results arc discussed in relation to the factors affecting blood pH in embryos at this stage of development.
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13.
  • 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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14.
  • (1)The preferred temperatures of Macrobrachium acanthurus were determined for prawns acclimated to 20°C, 23°C, 26°C, 29°C and 32°C, and the final preferendum estimate was (29.5°C).
  • (2)The critical thermal minima (CTMin) and maxima (CTMax) were 11.0°C, 12.1°C, 13.0°C and 14.8°C, and 34.2°C, 35.0°C, 36.1°C and 39.8°C, respectively.
  • (3)The zone of thermal tolerance assessed using the CTMin and CTMax boundaries was 644°C2.
  • (4)The acclimation response ratio was between 0.33 and 0.62.
  • (5)To cultivate this species in the southeastern region of México it should be done in not <15°C (CTMin) during the winter and below 38°C in summer (CTMax).
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15.
  • 1.1. Resting oxygen consumption at 10°C did not change from normoxia (150 mm Hg) down to an oxygen tension of 55 mm Hg for the flounder, Platichtys flesus.
  • 2.2. Flounders exposed to hypoxia showed increased levels of blood glucose and lactate, dependent on the degree of hypoxia.
  • 3.3. Due to hypoxia glycogen was depleted in the liver and swimming muscle but in the heart there was no significant change.
  • 4.4. Liver glucose increased after 7 hr of hypoxia. Heart and muscle glucose did not change but the absolute glucose concentration in the heart was five times higher than in the muscle.
  • 5.5. There is a transient accumulation of lactate in heart, liver and kidney after 7 hr of hypoxia while lactate accumulation in the swimming muscle is significant only after 21 hr of hypoxia.
  • 6.6. Succinate only accumulated in the liver while alanine accumulated in muscle, heart and liver.
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16.
  • 1.1. Preparation, purification and characterization of a phosphoglycolate phosphatase (PGP)3 isoenzyme from human erythrocytes was achieved by DEAE-Sepharose CL.-6B chromatography and isoelectric focusing using carrier ampholytes. pH 4–6.
  • 2.2. The isoenzyme has an isoelectric point of 5.00 ± 0.05 and could be purified 33.000 fold to a specific activity of 32.7 U/mg of protein. It represents the PGP phenotype 1 consisting of a single isoenzyme.
  • 3.3. The enzyme is composed of two subunits (mol. wt 35,000) which are identical and not connected by SS-bridges.
  • 4.4. At 4°C the isoenzyme is more stable in the pH range of 7–9 than at acid pH values.
  • 5.5. Incubation at 30 and 40°C for 4 hr does not affect the activity of the isoenzyme.
  • 6.6. It has a Km-value of 0.28 mM for phosphoglycolate (PG) as substrate.
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17.
  • 1.Male Uca pugilator whose major cheliped was immersed in 3 °C water bath experienced a significant drop in Tb. Thus, the enlarged claw of male Uca pugilator may have an unexplored function: thermoregulation.
  • 2.Crabs prefer warmer substrates (19–24 and 28–30 °C) over cooler (15–17 °C).
  • 3.Mean selected temperature (MST) may not be an accurate reflection of Tb. Crabs in a thermal chamber preferred temperatures between 25 and 30 °C but their average Tb was 23.2 °C.
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18.
  • 1.1. Active transport of d-glucose was shown using intestinal sac preparations, in vitro, made from two marine fish, the scup, Stenotomus versicolor and the puffer, Spheroides maculatus.
  • 2.2. Differences in absorption characteristics were evident in populations from year to year.
  • 3.3. Anaerobiotic conditions, i.e. 100 per cent nitrogen gassing of the incubation medium, inhibit the active transport of d-glucose in scup and puffer intestine.
  • 4.4. Phlorizin, 5 × 10−4 M, inhibits the active transport of d-glucose in scup intestine.
  • 5.5. Intestinal transmural glucose transport mechanisms operate well at incubation temperatures, 20°–27°C, i.e. temperatures close to habitat and holding tank temperatures, whereas movement of the sugar against a concentration gradient is interrupted at higher incubation temperatures, 29° and 30°C.
  • 6.6. Detailed comparison of procedures and results with those used by other workers in the field of in vitro intestinal absorption of poikilotherms suggests that aerobic metabolism may not be a uniformly significant energy source in intestinal active transport.
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19.
  • 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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20.
  • 1.1. 14C-dichlorofarnesoate permeated rapidly into Haemonchus contortus (infective juveniles) and Panagrellus redivivus (mixed cultures) and was strongly bound by hydrophobic association (Ks > 10−4M).
  • 2.2. Uptake rose linearly with increases in temperature (5–38°C) and external concentration (C0; 0.07–2.15 × 10−4 M). Within 1 hr the internal concentration, C1 was >C C0.
  • 3.3. The pH of the medium (6–8) did not affect uptake.
  • 4.4. Efflux of dichlorofarnesoate was low: the half-time of release was > 18 hr.
  • 5.5. The uptake curve approximated to the expression C1/C0 = a(1 − e−bt) with a and b as constants and t in hr.
  • 6.6. These results clarify previous work on the inhibitory action of juvenile hormone on the development of nematodes.
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