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1.
  • 1.1. Both the small riparian skink Sphenomorphus quoyii and its completely terrestrial relative Ctenotus robustus respond to forced submergence with instantaneous bradycardia.
  • 2.2. The strength of the bradycardia was affected by water temperature and fear. Dives into hot (30°C) water produced weak and erratic bradycardia compared to dives into cold (19.5°C) water. For S. quoyii the strongest bradycardia occurred when submergence took place in water at a lower temperature than the pre-dive body temperature.
  • 3.3. Upon emergence both species of skink exhibited elevated heart rates and breathing rates while heating from 19.5 to 30°C, compared to heating at rest. The increased heart and breathing rates probably act to replenish depleted oxygen stores and remove any lactate. Increased heart and ventilation rates are not indicators of physiological thermoregulation in this case.
  • 4.4. Both lizard species exhibited higher heart rates and ventilation frequencies during heating than cooling.
  • 5.5. Compared to its terrestrial relative, S. quoyii does not appear to possess any major thermoregulatory, ventilatory or cardiovascular adaptations to diving. However, very small reptiles may be generally preadapted to use the water to avoid predators.
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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. 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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4.
  • 1.1. A purification procedure for a thioredoxin from the extremophilic archaeon Sulfolobus solfataricus is described.
  • 2.2. The thioredoxin is active in the dithiothreitol-dependent reduction of insulin disulfide bonds.
  • 3.3. The thioredoxin is a monomer of 24,800 Da; it is an acidic protein with a pi of 4.5.
  • 4.4. The protein is stable to heating for 3 hr at 90°C.
  • 5.5. The amino acid composition of S. solfataricus thioredoxin is reported.
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5.
  • 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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6.
  • 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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7.
  • 1.Measurements of body temperature (Tb) in the field demonstrate that Platypedia putnami var. lutea Davis regulates Tb through behavioral mechanisms.
  • 2.Thermal responses (minimum flight temperature 17.3°C, maximum voluntary tolerance-temperature 32.5°C, and heat torpor temperature 44.4°C) of P. putnami var. lutea are related to the altitude of their habitat.
  • 3.Water loss rates increase with ambient temperature (Ta). Water loss rates are not significantly different at the extremes of the active Tb range but increase significantly when exposed to elevated Ta.
  • 4.Acoustic activity was restricted at 6.7°C Tb range. This is similar to the lower end of the Tb range for singing measured in cicada species that produce sound with a timbal mechanism.
  • 5.The use of the wing musculature to produce acoustic signals in P. putnami var. lutea does not increase the Tb range over which the species can call compared to timbal calls produced by other cicada species.
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8.
  • 1.1. The effects of thermal acclimatization at 10 and 24°C on heart rate were investigated on unrestrained soles (Solea vulgaris).
  • 2.2. The sensitivity of heart rate to temperature changes induced by temperature acclimatization was higher in cold-acclimatized than in warm-acclimatized soles.
  • 3.3. Heart rate of cold-acclimatized fish to temperature changes was not affected by blocking the vagal tone with atropine.
  • 4.4. After atropine treatment the ability of heart rate to show thermal compensation decreased in warm-acclimatized soles.
  • 5.5. It is suggested that the vagus nerve can function differently at different temperatures.
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9.
  • 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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10.
  • 1.1. External and internal examinations of otoliths in fishes for macrostructure and microstructure has demonstated yearly, daily and population rhythmic patterns.
  • 2.2. Chemical analyses (atomic absorption) of otolith carbonate from reared Fundulus heteroclitus for strontium-calcium concentration ratios demonstrated changes in chemistry related to temperature.
  • 3.3. Microprobe analyses made it feasible to interpret almost daily changes in temperature to provide the temperature history of an individual fish.
  • 4.4. A combination of microprobe analyses and daily increment analyses of otoliths can provide a life history profile for individual fish and can provide information on the environmental history of each fish.
  • 5.5. Such information is vital to our understanding of the processes underlying recruitment and growth rates, and would make it possible to link growth and mortality rates to environmental occurrences.
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11.
  • 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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12.
  • 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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13.
  • 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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14.
  • 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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15.
  • 1.1. The temperature dependence of the kinetics of the yeast AM P deaminase was examined using the purified enzyme and the permeabilized yeast cells.
  • 2.2. The increase in the enzyme affinity for the substrate AMP was accompanied by the decrease in the maximal velocity with the decreasing temperature in the absence and presence of ATP.
  • 3.3. The apparent Km for AMP was lowest at 15–20°C, and the affinity was decreased below and above this temperature.
  • 4.4. The rate of the AMP deaminase reaction remained constant over a wide range of temperature in the presence of physiological AMP concentrations.
  • 5.5. The temperature dependent change in kinetic properties of AMP deaminase may contribute to the control of the yeast glycolytic flux under the condition of lower temperature environments.
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16.
  • 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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17.
  • 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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18.
  • 1.1. Kinetic constant values of the reaction catalyzed by bass liver glucose 6-phosphate dehydrogenase show to be modified between 10 and 40°C.
  • 2.2. The Arrhenius plot between 10 and 50°C shows two slopes with different activation energies.
  • 3.3. These results suggest a regulation of this enzyme by environmental temperature.
  • 4.4. Kinetics of ATP inhibition were examined between pH 6.2 and 7.8: patterns and Ki values obtained are affected by the pH variation.
  • 5.5. NADH is an effective inhibitor of bass glucose 6-phosphate dehydrogenase but this enzyme does not show NAD-linked activity.
  • 6.6. Kinetics of pyridoxal 5′-phosphate inhibition have indicated the presence of a lysine in the catalytic site for NADP+.
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19.
  • 1.1.|Hyperthermia (c. 41°C) occurs in mammals (e.g. humans) during normal life-history events such as fever and vigorous exercise. The effects of such episodic hyperthermia on early developmental stages of cancer are of potential importance, yet have been investigated hardly at all.
  • 2.2.|We injected female Sprague-Dawley rats with the mammary-gland carcinogen 7,12-dimethylbenzathracene and, over a 4-week period before cancer onset, subjected them to 20 1-h episodes of whole-body hyperthermia (41.2°C colonic) to determine effects on subsequent appearance of carcinomas.
  • 3.3.|Hyperthermia did not have significant effects on the development of clinical disease in this system, indicating that precancerous or incipient cancerous cells are not susceptible to damage by the levels of hyperthermia associated with normal life-history events.
  • 4.4.|For repeated induction of hyperthermia with minimal confounding effects of stress, we refined a technique in which hyperthermia-treated animals, as well as controls, were anesthetized with sodium pentabarbital during thermal treatments, thus suppressing thermoregulation and higher brain functions.
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20.
  • 1.1. Metabolic rates (ml O2/mg/hr) of three geographically separated populations of the carabid beetle Calathus melanocephalus L. (Finse and Je 10y, Norway and Drenthe, The Netherlands) were measured and compared by ANCOVA.
  • 2.2. No significant relationship (P > 0.05) between metabolic rates and body weight or sex of the animals were found.
  • 3.3. Individuals mostly acclimated to low temperatures by increased metabolic rates and in the opposite direction to higher temperatures. Individuals collected in early summer also showed higher metabolic rates than those caught later in the autumn.
  • 4.4. Contradicting the theory of metabolic cold adaptation, beetles from The Netherlands had the highest metabolic rates, beetles from Finse intermediate rates and beetles from Jeløy the lowest rates.
  • 5.5. No significant relation were found between geographical origin of the beetles and their respective chill-coma temperature.
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