The dependence of oxygen consumption of the common whelk (Buccinum undatum) on hypoxia,salinity and air exposure

• 1.1. Oxygen consumption of low salinity (20‰) acclimated whelks decreases markedly upon acute exposure to hypoxia (P_WO₂ = 35 Torr), but almost regenerates its original level within 48 hr exposure to the hypoxic condition.
• 2.2. This ability to regain the original level of oxygen consumption is not seen in high salinity (35‰) acclimated whelks.
• 3.3. Oxygen consumption in air at 10°C is more than twice the rate shown by low salinity acclimated whelks in normoxic water (P_WO₂ = 150 Torr).
• 4.4. Q₁₀ for oxygen consumption in air is about 1.0 in the temperature range 10–20°C.

     

Laboratory studies on the oxygen consumption of the marine teleost,Lichia amia (Linnaeus, 1758)

• 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.

     

Oxygen debt in reptiles: Relationship between the time required for repayment and metabolic rate

• 1.1. The increase in O₂ consumption in a 5 g lizard (Anolis carolinensis) after feeding and after maximal work was compared with that in a kilogram alligator (Alligator mississippiensis) treated similarly.
• 2.2. The amount of extra O₂ consumed/kg was the same in both. At the peak, there was a 2.6 fold increase in both animals following exhaustive work. Oxygen usage was elevated for 2 hr in the lizard and for 12 hr in the alligator, in inverse proportion to their respective metabolic rates.
• 3.3. Although the extra oxygen consumed was the same. feeding increased metabolic rate at the maximum by 300% in the alligator and by only 40% in the lizard.

     

Factors affecting oxygen consumption in wild-caught yellow-bellied marmots (Marmota flaviventris)

• 1.1. All age groups gained mass during the active season, but mass-gain of adult females was delayed during lactation.
• 2.2. The relationship of body mass to metabolic rate varied widely; when the relationship was significant, R² varied from 10.3 to 72.6%. Body mass affects V_O2 more during lactation than at any other period.
• 3.3. Mean VinO₂ of adult males was higher in June than that of adult, non-lactating females.
• 4.4. V_O2 of reproductive females was significantly higher during lactation than during gestation or postlactation because specific V_O2 varied. Specific V_O2 of non-reproductive females declined over the active season.
• 5.5. Specific V_O2 of all age groups declined between the premolt and postmolt periods. The reduced maintenance costs can contribute 20–46% to daily growth.
• 6.6. Observed V_O2 was lower than the value predicted from intraspecific or interspecific Bm:M regressions.
• 7.7. V_O2 of wild-caught marmots was lower than that of marmots maintained in the laboratory, probably because of dietary differences.
• 8.8. Because basal metabolism is a stage on a food-deprivation curve, we suggest that basal metabolic rate is not an appropriate measure of the metabolic activity of free-ranging animals.

     

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.

     

Effects of exercise-stress on ventilation,cardiac output and blood respiratory parameters in the carp,Cyprinus carpio

• 1.1. Carp (Cyprinus carpio) were stressed to exercise by rolling in a respiration chamber. Ventilatory water flow rate, cardiac output and blood respiratory parameters were determined.
• 2.2. During exercise, oxygen uptake increased about 3.5-fold and returned to pre-exercise level within 15 min.
• 3.3. This exercise-stress resulted in no plasma acidosis and in no swelling of the erythrocytes.
• 4.4. Ventilatory water flow rate increased 6-fold, whereas cardiac output increased 2-fold. Hence the ventilation-perfusion ratio increased during exercise.
• 5.5. During exercise, arterial O₂ content (CaO₂) increased due to increases in O₂ tension (PaO₂), O₂ saturation of hemoglobin (SaO₂) and hemoglobin concentration (Hb). On the other hand, Pv̄O₂ and Sv̄O₂ remained at the resting levels but Cv̄O₂ slightly increased due to an increase in Hb.
• 6.6. Arterial-venous O₂ difference (CaO₂-Cv̄O₂) increased by 38%, which was met by a much greater increase in CaO₂ than Cv̄O₂.

     

The effects of environmental variables on the heart rates of invertebrates

• 1.1. The effects of temperature, salinity and declining O₂ on the heart rates of nine species representing four animal phyla have been investigated in relation to other respiratory paramters.
• 2.2. The effect of temperature on heart rate is at least the same as, and often greater than, the effect of temperature on O₂ consumption, thus providing no evidence that adaptations of the cardiovascular system facilitate metabolic compensations for a temperature change.
• 3.3. Responses to reduced acclimation salinity are very diverse among the various species, permitting no general conclusions about the role of the cardiovascular system in adaptations to estuarine habitats.
• 4.4. At low PO₂ the typical response is bradycardia, which is especially notable in species with a high capacity for anaerobic metabolism. Compensatory tachycardia, the expected response in vertebrates, is very rare in other animal groups.
• 5.5. Estimates of cardiac output from these data generally agree with those obtained according to the Fick principle from blood gas tensions.
• 6.6. The estimates of cardiac output are evaluated in terms of body size, temperature and the design of cardiac muscle, which is fundamentally different in various animal phyla.

     

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 influences of individual variations in metabolic rate and tidal conditions on the response to hypoxia in Carcinus maenas (L.)

• 1.1. The oxygen consumption of crabs in normoxic and hypoxic (50% O₂) seawater was measured directly after collection.
• 2.2. The influences of size and lunar cycles were removed by scaling the data.
• 3.3. Strong negative correlations between low individual levels of O₂ consumption and the ability to compensate for hypoxia were apparent in Wicklow (subtidal) crabs.
• 4.4. Compensation for hypoxia was much greater on the flood tide than on the ebb.
• 5.5. Crabs from Roscoff (intertidal) had lower levels of compensation than those from Wicklow.
• 6.6. Size, sex and condition had no apparent effect upon these relationships.
• 7.7. Crabs acclimated to laboratory conditions have not shown this tidal variation in compensation for hypoxia.

     

The effect of salinity and ion composition on oxygen consumption and nitrogen excretion of Macrobrachium rosenbergii (de man)

• 1.1. Oxygen consumption and nitrogen excretion rates of Macrobrachium rosenbergii were recorded in media of varying salinities and ion compositions (Mevo Hamma, Yahel, Elat—continental water; and 15 and 24%. seawater dilutions).
• 2.2. Oxygen consumption rates were not significantly different (P > 0.05) with the exclusion of Yahel having a metabolic rate of 0.258ml O₂/gfw/hr which was significantly different from the other experimental media at the P ≲- 0.05 level.
• 3.3. Nitrogen excretion rates were lowest in prawns adapted to Yahel water, 0.0188mg NH₄-N/gfw/hr and increased with salinity to 0.0494mg NH₄-N/gfw/hr in 24%.
• 4.4. The O: N ratios ranged from 12.24 to 22.65 indicating that in dilute media (Mevo Hamma and Yahel) relative to saline media (15%, Elat and 24%) more lipids and carbohydrates are utilized as an energy substrate while the latter group increased protein catabolism.

     

Effect of experimental ventilation of the skin on cutaneous oxygen uptake in the carp,Cyprinus carpio

• 1.1. Cutaneous O₂ uptake in the carp, Cyprinus carpio, was determined at various water flow rates across the skin (.V) ranging from 2.5 to 40 ml/min, using flow-through respirometers.
• 2.2. When thickness of water flow was 2mm, cutaneous O₂ uptake remained stable (about 3.8 nmol/cm²/min) at a .V of 20–40 ml/min and decreased with .V below 20 ml/min.
• 3.3. When thickness of water flow was 4 mm, cutaneous O₂ uptake decreased with .V below 40 ml/min.
• 4.4. Apparent water velocity (U') was calculated dividing .V by an area of a cross section of the water flow (0.5 and 1.0 cm² respectively). In both experiments, cutaneous O₂ uptake decreased with U' below 0.7 cm/sec.
• 5.5. This suggests that cutaneous O₂ uptake in the carp is limited at a low water velocity by a resistance of the hypoxic boundary layer.

     

Running performance of the thirteen-lined ground squirrel,the eastern chipmunk and the albino Norway rat

• 1.1. The procedure used to compare the forced running performance of three rodent species was the number of electrical stimuli required each minute to keep the animals running.
• 2.2. During running trials, ground squirrels, Spermophilus tridecemlineatus, required fewer stimuli than white rats. Squirrels ran 12.4 ± 6.9 (2 SE) min before requiring stimulation vs 3.1 ± 1.4 min for rats.
• 3.3. Total oxygen consumption during the running period was significantly higher for ground squirrels than white rats, 4.70 ± 0.36 and 4.18 ± 0.38ml O₂/g/hr, respectively.
• 4.4. Heart weight/body weight ratios were significantly higher for the ground squirrels than the white rats.
• 5.5. No differences were noted between ground squirrels and chipmunks other than those which could be accounted for by body weight differences.

     

A note on eggshell porosity,nest humidity and the effects of DDE in the grey heron (Ardea cinerea)

• 1.1. Water vapour conductance (G_H2O) 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 G_H2O 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 (ΔP_H2O), 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.

     

Specific dynamic action (SDA) in the supralittoral isopod,Ligia pallasii: Relationship of growth to SDA

• 1.1. The relationship of Specific Dynamic Action (SDA) to growth was examined in the supralittoral isopod Ligia pallasii using a seaweed diet fed at different rations.
• 2.2. Animals increased in live weight by 33% on an ad libitum or 100% diet and by 2% on a 20% ration over a 10-week period.
• 3.3. Weight-specific VO₂ was significantly higher in animals eating the 100% diet than in ones eating the 20% diet. Decline in VO₂ with time in animals on the 20% diet was probably due to poor health associated with a maintenance ration.
• 4.4. SDA per unit weight of food eaten was 18% higher in the 20% diet group than in the 100% one, and values remained constant over time in both groups.
• 5.5. k₁ growth efficiencies (production/consumption) were higher in animals on 100% ration than in ones on 20% ration. Efficiencies declined with time in both diet-groups and fell below zero in the 20% ration-group, coincidental with weight-loss in some of the animals.
• 6.6. Overall SDAs for the 10-week period were positively correlated with growth (r₂ = 0.77), but there was no way to separate this from amounts eaten as an effect on SDA.

     

The oxygen consumption rates of three gastrotrichs

• 1.1. The oxygen consumption rates for three sympatric species of marine gastrotrichs (anatomically similar, except that one contains hemoglobin) were measured with a Cartesian diver microrespirometer.
• 2.2. The rates for the two species without hemoglobin, Turbanella ocellata and Dolichodasys carolinensis, were 307.2 μl O₂ g⁻¹ hr⁻¹ and 108.0 μl O₂ g⁻¹ hr⁻¹, respectively, while the rate for the hemoglobin-containing species, Neodasys, was 208.9 μl O₂ g⁻¹ hr⁻¹.
• 3.3. The possession of hemoglobin by Neodasys (14% by volume) cannot be explained by an unusually high demand for oxygen.
• 4.4. Instead, the hemoglobin may be useful as an oxygen store providing continued aerobic metabolism in anoxic conditions, thus allowing Neodasys to exploit a different niche.

     

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.

     

Effects of water stress on hemolymph volume,osmotic potential and chemical composition in Megetra cancellata

• 1.1. Rates of water loss in Megetra cancellata were very high compared to those reported for other xeric arthropods.
• 2.2. Hemolymph weight in hydrated animals was 43.0% of the total body weight while it was 24.7% in desiccated animals that had lost 16.1% of their body weight as water.
• 3.3. Hemolymph osmotic potential increased from 417 to 447 mOsm/kg in desiccated beetles, but osmotic regulation was evident.
• 4.4. Total hemolymph protein mass and concentration decreased in desiccated beetles while amino acid concentrations remained constant (at about 70 mM).
• 5.5. Na⁺ and −PO₄ concentrations increased in desiccated beetles.
• 6.6. Cl⁻ and K⁺ concentrations in desiccated beetles were equal to those in undesiccated beetles.

     

Gas tensions within the egg of the quail (Coturnix c. Japonica) during the closing stages of embryonic development

• 1.1. The respiratory status of the embryonic quail during the two days prior to hatching was assessed by measuring the gas tensions within the air space of the egg and of blood collected from the chorioallantois.
• 2.2. When the lungs became inflated there was a significant decrease in the pO₂ of the gas in the air space.
• 3.3. After pipping, there was a rise in the pO₂ and fall in the pCO₂ within the air space, together with corresponding changes in the blood.
• 4.4. The outer shell membrane remained intact until the onset of hatching.
• 5.5. These results were compared with those obtained by other workers using the domestic fowl.

     

Effect of size and temperature on the oxygen consumption of the brown shrimp Penaeus californiensis (Holmes, 1900)

• 1.1. The routine rate of oxygen consumption by Peneaus californiensis was determined for the size groups with average weights of 0.26, 2.31 and 10.01 g at five temperatures (19, 23, 27, 31 and 35°C).
• 2.2. Oxygen consumption (mg O₂/g min) was independent of dissolved oxygen (DO) level down to 1.8mg/l, increased with temperature (P < 0.05) from 0.0015mg O₂/g min for the preadults at 19°C to 0.0106 mg O₂/g min at 35°C for the postlarvae, and was inversely proportional to weight (P < 0.05).
• 3.3. The thermal coefficient (Q₁₀) indicated a higher sensitivity by preadults to temperature variations.

     

Oxygen consumption and torpor in the fat-tailed dwarf lemur (Cheirogaleus medius): Rethinking prosimian metabolism

• 1.1. Oxygen consumption was measured in a lemuriform prosimian, Cheirogaleus medius. throughout a 24-hr cycle. The standard metabolic rate was determined to be 0.95 ml O₂ (g · hr)⁻¹ agreeing well with the value predicted by allometric equations, 0.91 ml O₂ (g · hr)⁻¹.
• 2.2. As a group, prosimians are argued to have metabolic levels in agreement with eutherian norms, rather than hypometabolic levels as previously supposed.
• 3.3. Day length is shown to be an important behavioral cue for this species. Its complex yearly and daily torpor cycles are linked to this stimulus.