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1.
2.
  • 1.1. Uptake of [14C]-labelled d-glucose, l-arabinose and d-fructose by intestinal and renal brush border and basolateral membrane vesicles was studied in the absence of Na+ .
  • 2.2. The Na+-independent d-glucose transport system in these membrane vesicles was saturable, sensitive to phloretin, stereospecific and accessible only to d-glucose and d-galactose.
  • 3.3. Na+-independent l-arabinose transport was not saturable even when its concentration was raised to 300 mM and it was insensitive to phloretin.
  • 4.4. Na+-independent d-fructose transport demonstrated saturation kinetics with only renal brush border membrane vesicles, but it was not inhibited by either phloretin or phlorizin.
  • 5.5. These studies indicated that the Na+-independent carrier-mediated d-glucose/d-galactose transport system of intestinal and renal brush border and basolateral membranes is clearly not shared by other monosaccharides.
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3.
  • 1.1. Glycogen, caffeine and glucose dissociate phosphorylase a tetramer to dimers with half-maximum effect at 0.16%, 1.1 and 71 mM concentration, respectively, as monitored by crosslinking with dimethyl suberimidate at 18°C.
  • 2.2. The above ligands increase the rate of dephosphorylation and tryptic digestion of phosphorylase a at 18°C in the same way with half-maximum effect at 0.04%, 0.1 and 9 mM concentration, respectively.
  • 3.3. Caffeine and glucose acted synergistically in tetramer dissociation as well as in the enzymic modifications.
  • 4.4. The α-anomer of d-glucose was twice as effective as its mutarotational equilibrium solution.
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4.
  • 1.1. Nicotine at 10 mM, but not caffeine or theophylline, reduced by 20% the overshoot of the Na+-dependent d-glucose transport in ratjejunal brush border membrane vesicles.
  • 2.2. Since nicotine did not affect the transport of Na+, its inhibition on Na+-dependent d-glucose transport must be due to a direct effect upon the d-glucose transport system.
  • 3.3. Folate transport in these membrane vesicles was found to a be a free diffusion process at pH 7.4.
  • 4.4. Neither caffeine, theophylline nor nicotine has any effect on folate transport.
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5.
  • 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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6.
  • 1.1. In 43 European bison divided into three groups (Group A, 3–8-month-old calves; Group B, 18-month-7-year-old young bison; Group C, 12–24-year-old bison) the rectal, humerus region and abdomen region temperatures were measured.
  • 2.2. The experiments were carried out in winter months, from mid-December to mid-March.
  • 3.3. The mean rectal temperatures changed from 38.55°C in calves to 38.15°C in the oldest bison.
  • 4.4. The mean temperatures of the humerus region changed from 20.69°C in calves to 21.49°C in older bison.
  • 5.5. The mean temperatures of the abdomen region changed from 20.79°C in calves to 22.17°C in older bison (Gr. B).
  • 6.6. The cluster analysis divided the bison into four groups named hot, warm, cool and cold bison.
  • 7.7. Only air temperature measured 2 m above the ground and snow cover influenced the integrated bison temperature. Age, sex and mass as well as some environmental factors had no influence.
  • 8.8. Measurements made 1 to nearly 4hr after a bison's death showed a drop in rectal temperature and mostly increases in temperatures of the humerus and abdomen regions.
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7.
  • 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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8.
  • 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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9.
  • 1.1. Coatis are chiefly diurnal, showing marked nycthemeral variations of body temperature and oxygen uptake.
  • 2.2. The thermoneutral zone extends from 25–33°C; the basal metabolic rate is about 40% below the value predicted from body mass.
  • 3.3. Thermoregulation in cold is excellent, partly due to decreasing thermal conductance at falling ambient temperatures.
  • 4.4. Exposure to temperatures above 35°C is endured for only short periods.
  • 5.5. Basal heart rate is reduced to about 70% of the predicted level. The contribution of heart rate to increased oxygen demands at falling ambient temperatures is rather low.
  • 6.6. The measured physiological characteristics of coatis are discussed with regard to the high mobility and the wide distribution range of these procyonids.
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10.
  • 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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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)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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13.
  • 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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14.
  • 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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15.
  • 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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16.
Absract
  • 1.1. The basal metabolism of the vole, Microtus ochrogaster, a non-hibernator is about 80% below that expected for microtine rodents, while the basal metabolism of the chipmunk, Tamias striatus, is about 20% below that expected for small mammals.
  • 2.2. Blocking thyroid secretion results in a 3°C improvement in the vole. and a 2°C improvement in the chipmunk, to the highest air temperature tolerated.
  • 3.3. Blood levels of thyroxine in both species did not change as a function of ambient temperatures, whereas rates of radioiodine release were reciprocally related to ambient temperature.
  • 4.4. There was no indication that the thyroid gland of the chipmunk was ever inactive either preceding, or during, hibernation.
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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. Norepinephrine-induced lipolysis, cyclic AMP production and glycerokinase activity were measured, in vitro, in the brown fat of rats born and reared at either 28° or 16°C during the first 3 weeks of life.
  • 2.2. During the first two postnatal days, lipolytic activity in the tissue was lower than in the foetuses at both ambient temperatures At day 10, increased values of the parameters under consideration were similarly observed in both groups.
  • 3.3. However, the hormonal regulation of lipolysis seemed to be quite different from that found in adult cold-acclimated rats.
  • 4.4. At day 21, the cold-induced characteristics of lipid metabolism in brown fat were observed in the 16°C exposed rats, whereas a loss of tissue stimulation occurred in the 28°C exposed ones.
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19.
  • 1.1.|The standard metabolic rates (SMRs) and preferred body temperatures (PBTs) of the tropical cordylid Cordylus jonesi and temperature lacertid Lacerta lilfordi were determined following acclimation to constant environmental temperatures of 20 and 30°C.
  • 2.2.|Although after 5 weeks the SMRs of Cordylus jonesi and Lacerta lilfordi displayed partial compensations of 20.9 and 10.5%, respectively, their PBTs did not alter over this period. Therefore, acclimation does not maintain complete metabolic homeostasis during either the active or inactive phase of the lizard.
  • 3.3.|Cordylus jonesi allowed to thermoregulate behaviourally at their PBT during activity possessed similar SMRs to control animals maintained continually at the same background temperatures, indicating that acclimation state in lizards is determined by the body temperatures experienced while at rest.
  • 4.4.|The particular acclimatory problems of animals exhibiting behavioural homeothermy are discussed.
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20.
  • 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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