The effects of acclimatization on body weight and oxygen consumption in Dipodomys panamintinus

• 1.1. Seasonal acclimatization effects on oxygen consumption, body temperature, and body weight were evaluated in three different experimental groups of Dipodomys panamintinus.
• 2.2. Body weights of wild field as well as captive animals housed in outdoor sand cages were maximum in winter and lowest in summer for both sexes.
• 3.3. Mean oxygen consumption was maximum in winter and lowest during spring in both sexes of the wild field and captive exposed groups.
• 4.4. Neither weight nor oxygen consumption of indoor control animals varied with the seasons.
• 5.5. No significant differences in body temperatures were observed during either the fall or winter seasons.

     

Contribution of aerobic and anaerobic scope to the total metabolic scope of the desert skink,Chalcides ocellatus (Forskal)

• 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.

     

Social facilitation of reduced oxygen consumption in Mus musculus and Meriones unguiculatus

• 1.1. The short-term resting rates of oxygen consumption of laboratory white mice (Mus musculus) and Mongolian gerbils (Meriones unguiculatus) were measured by closed system manometry.
• 2.2. Metabolic rates of animals tested individually were compared to those of huddled trios and trios in which the animals were tested simultaneously but prevented from physical contact (separated trios) at temperatures ranging from 9–25° C.
• 3.3. Rates of increase of weight-specific resting metabolism were greatest for animals tested individually.
• 4.4. There was no significant difference in the rates of increase of oxygen consumption between huddled and separated trios in cither species.

     

Oxygen consumption and production by tropical ascidians symbiotic with Prochloron

• 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.

     

The changes in body temperature,oxygen consumption,CO2 production and muscle protein turnover rate by selection for body size in Japanese quail,Coturnix coturnix japonica

• 1.1. Body temperature, oxygen consumption, CO₂ production and muscle protein degradation rate were measured in the three quail lines selected for body size, a random bred line (RR) and two lines selected for large (LL) or small (SS) body size.
• 2.2. The body temperature at 15 weeks of age was highest for small body size line and lowest for large body size line.
• 3.3. The body temperature, oxygen consumption and CO₂ production of females were significantly higher than that of males.
• 4.4. The fractional degradation rate of muscle protein of SS, RR and LL lines were measured as 2.4, 1.6 and 1.2% per day in male, and 2.6, 1.7 and 1.4% per day in female.

     

Utilization of body stores in embryonated ova and larvae of two coregonid species (Coregonus lavaretus L. and C. albula L.)

• 1.1. Developing eggs of whitefish (Coregonus lavaretus L.) and vendace (Coregonus albula L.) were kept at 1–2°C and some eggs taken gradually up to 8°C to provoke mass hatching of embryos.
• 2.2. Wet weight, dry matter and the contents of lipid, protein and ash were measured in fish during the course of experiment.
• 3.3. Dry matter content decreased gradually in whitefish eggs from 15.64 to 11.95% during 1 month at 1–2°C, whereas vendace eggs showed only a slight decrease from 16.27 to 15.53%.
• 4.4. In both species protein content decreased but lipid increased when approaching the natural time of hatching.
• 5.5. During delayed hatching at low water temperatures protein contributes to catabolism, whereas lipid content decreased only in the later phase of the experiment.
• 6.6. Larvae starved for 10 days after hatching lost increasing amounts of dry matter (from 26.1 to 50.3% of body weight) and protein (from 18.7 to 45.9% of body weight) as they remained longer in cold water as embryos.
• 7.7. A correspondence was found between assessment of metabolic utilization of body stores based on chemical analysis of fish body and previous work on oxygen consumption and nitrogen excretion.

     

Effects of low environmental pH and temperature on hatching and metabolic rates in embryos of Anax junius drury (Odonata: Aeshnidae) and the role of hypoxia in the hatching process

• 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.

     

Effect of eyestalk ablation on oxygen consumption of callinectes similis exposed to salinity changes

• 1.1. The effect of eyestalk ablation on preadults of Callinectes similis exposed to a constant salinity (30%.) and to simulated tidal changes in salinity (30-11 to 30%.) were measured.
• 2.2. In constant salinity, crabs showed a persistent respiratory rhythm, with a maximum oxygen consumption during the day. Under these conditions, ablation significantly increased the respiratory rate but not the rhythm.
• 3.3. In variable salinities, the highest respiratory rates occurred in salinities of 11 and 16%. during the night. In these crabs, ablation of eyestalks and subsequent injection of eyestalk extracts did not alter the respiration rate rhythm.
• 4.4. The circadian rhythm is controlled by the periodicity of environmental changes instead of the influence of eyestalk hormones.
• 5.5. Regulation of metabolism in C. similis associated with osmoregulation involves other neurosecretory organs.

     

Metabolic rates of Calathus melanocephalus (L.) (coleoptera,carabidae) from alpine and lowland habitats (jeløy and finse,norway and drenthe,the netherlands)

• 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.

     

Effects of temperature and acid stress on hatching,survival capacity,metabolism and postural reflexes in caenid mayflies (ephemeroptera)

• 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.

     

Effect of temperature and salinity on the oxygen consumption of laboratory produced Penaeus californiensis postlarvae

• 1.1. The oxygen consumption by P. californiensis postlarvae (mean wt = 0.38 g) was determined at five different temperatures and four salinities.
• 2.2. The O₂ in each chamber was recorded at 10 min intervals for 1 hr. The time course of oxygen depletion was independent of O₂ concentration down to 1.6 mg/l.
• 3.3. Oxygen consumption increased with temperature from 0.0045 mg/g/min at 19°C, to 0.0142 mg/g/min at 35°C. The thermal coefficient (Q₁₀) indicated a very high sensitivity of the postlarvae to temperature variations at 19–23°C.
• 4.4. The results show that oxygen consumption significantly depends on temperature (P < 0.001) while salinity has only a marginal effect.

     

Thermal acclimation of metabolism and preferred body temperature in lizards

• 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.

     

Variations in response to environmental hypoxia of different colour forms of the shore crab,Carcinus maenas

• 1.1. The oxygen consumption of red and green Carcinus in normoxic and hypoxic sea water was determined, using an oxygen electrode in a sealed respirometer.
• 2.2. The red crabs had significantly higher “excited” oxygen uptake rates and a lower ability to compensate for hypoxia than the green crabs.
• 3.3. Red Carcinus display an emersion response to declining oxygen at lower oxygen tensions than the green crabs.
• 4.4. Mortality of red crabs exposed to prolonged anoxia was much greater.
• 5.5. The relationship of these findings to the zonation of the two colour forms on the shore is discussed.

     

Oxygen consumption,body temperature and heart rate in the coati (Nasua nasua)

• 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.

     

Respiratory mechanisms and metabolic adaptations of an intertidal crab,Chasmagnathus granulata (Dana, 1851)

• 1.1. The ventilatory mechanism, gill area, sites of oxygen uptake, oxygen consumption and activity of a crab from south Brazil, Chasmagnathus granulata, were investigated.
• 2.2. The oxygen uptake seems to be restricted to the gill lamellae.
• 3.3. The gill area varies with the wet body weight, being relatively higher in smaller animals. There is not a significative reduction of the gill area in relation to species of the infralittoral zone.
• 4.4. C. granulata presents a mechanism for recirculating the water of its branchial chamber when exposed to atmospheric air.
• 5.5. The oxygen consumption and activity are reduced when the animals are exposed to atmospheric air. The reduction in the oxygen consumption may be related to the poorly adapted respiratory system, while the decrease in activity may be a mechanism for saving energy during this hypoxic period.

     

The effects of temperature on oxygen consumption in Bullia digitalis meuschen (Gastropoda,Nassaridae)

• 1.1. The oxygen consumption of Bullia digitalis from South Africa's west coast, measured at a fixed activity level at 15°C, does not differ significantly between winter and summer.
• 2.2. The adult acute rate-temperature curve is flattened over the temperature range likely to be encountered in the field, there being no significant difference in oxygen consumption between 15 and 22.5°C.
• 3.3. Below this plateau the Q₁₀ is normal, giving a value of 2.67 between 5 and 10°C, but at temperatures above 22.5°C the Q₁₀ is less than 2 and oxygen consumption at 30°C does not approach that of the tropical Bullia melanoides at the same temperature.
• 4.4. Both field and laboratory acclimated animals provide evidence that the rate-temperature curve is unaffected by such acclimation, either to high or low temperatures.

     

Specific dynamic action (SDA) in the supralittoral isopod,Ligia pallasii: Effect of ration and body size on SDA

• 1.1. Ration and body size effects on specific dynamic action (SDA) were investigated in the supralittoral isopod Ligia pallasii using seaweed and chemical diets.
• 2.2. SDA increased asymptotically with ingested meal size for all diets.
• 3.3. Body weight had a significant positive effect on SDA for only one of the six diets tested, but weak tendencies were present in the data for the other diets.
• 4.4. SDA appeared to increase geometrically with increasing concentration of amino acids at high ration levels.

     

Temperature acclimation in respiratory and cytochrome c oxidase activity in common carp (Cyprinus carpio)

• 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.

     

Osmoregulation and temperature effects on water loss and oxygen consumption in two species of african scorpion

• 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.

     

Changes in the EEL intestine during seawater adaptation

• 1.1. Rate of fluid absorption by eel (Anguilla rostrata) intestinal sacs in vitro reached seawater adapted values 3 days after transfer from freshwater to seawater.
• 2.2. After 3 days in seawater oxygen consumption and Na-K-ATPase activity of intestinal mucosa had not increased over freshwater values.
• 3.3. The weight of intestinal mucosa increased 32% during seawater adaptation as a result of an increase in the number of mucosal cells (hyperplasia).
• 4.4. The rate of intestinal fluid absorption was reduced by 10⁻⁴ M ouabain and was not affected by 10⁻⁴ M acetazolamide.