Oxygen consumption and respiratory behaviour of three Nile fishes

1. The respiratory behaviour and patterns of oxygen consumption of three Nile species have been investigated.
2. Tilapia nilotica showed a typical pattern of oxygen consumption with an ambient region, adaptive plateau and lethal region (Fig. 2).
3. Specimens of Polypterus senegalus and Clarias lazera (body weights 20–30 and 30–45 g respectively) showed patterns of consumption comparable to that of Tilapia (Fig. 3a and 4a). In larger specimens of the two species the adaptive plateau was either insignificant or completely absent.
4. Specimens of Polypterus and Clarias (20–30 g and 30–45 g respectively) could survive in waters saturated with oxygen (7.4 mg/l) but their tolerance to lower oxygen concentrations was limited. Larger specimens of Polypterus and Clarias failed to survive in oxygen saturated waters.
5. The tolerance of Tilapia nilotica to extremely low oxygen concentration is an adaptation of a tropical and completely aquatic species. Polypterus and Clarias resort to their compensatory mechanisms only when the aquatic respiratory surface fails to satisfy their oxygen requirements.

     

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.

     

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.

     

Oxygen uptake in larval bollworms (Heliothis zea) infected with the fungus Nomuraea rileyi

• 1.1. Healthy 6- to 12-day-old Heliothis zea (bollworm) larvae showed a mean oxygen uptake of 3.1 μl O₂/mg body wt per hr.
• 2.2. Similar larvae infected with the fungus Nomuraea rileyi had a mean uptake of 4.01 μl O₂/mg per hr.
• 3.3. The weights of the two groups of insects did not differ.
• 4.4. T-test showed a significant (P < 0.01) difference in oxygen uptake between healthy and infected larvae.

     

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.

     

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.

     

Oxygen consumption of the larvae of the decapod crustaceans,Emerita talpoida (say) and Libinia emarginata leach

• 1.1. The oxygen consumption (V_o2) of laboratory reared Emerita talpoida and Libinia emarginata was measured at 5°C intervals (15–35°C).
• 2.2. The V_o2 of E. talpoida larvae was twice that of similarly sized L. emarginata larvae.
• 3.3. The maximum V_o2 for both species was at 25°C. but E. talpoida—older than stage III—had maximum rates at 30°C.
• 4.4. E. talpoida cultured at 25 or 30°C had a similar V_o2.
• 5.5. Growth, but not molting, stopped at Stage VI zoea in E. talpoida but the V_o2 diminished after these molts.

     

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.

     

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.

     

Effects of salinity and temperature on oxygen consumption in a freshwater population of Palaemonetes antennarius (Crustacea,decapoda)

• 1.1. After step-like increases in salinity the shrimps exhibit the smallest increase in oxygen consumption in the lower salinity range. At higher salinities the shrimps show longer recovery times and greater increases in the metabolic rate after salinity shock.
• 2.2. In steady-state experiments, the shrimps display the lowest oxygen consumption rates near the isosmotic point. The lowest metabolic rates occur at salinities of 3‰ and 10‰ At salinities of 20‰ and above the rate of metabolism increases by 20–30%.
• 3.3. The calculated osmoregulatory work for animals in fresh water amounts to only 2.7% of routine metabolism and drops to 1.1% for shrimps in 3‰ and 0.7% in 5‰ salinity.
• 4.4. Locomotory activity in the form of position change was not responsible for the increased oxygen consumption of the animals after salinity shocks. A “tentative swimming activity” by fast and frequent beating of the pleopods without position change may be an important factor in the increase of metabolic rates.
• 5.5. In its temperature response, the brackish water population has a higher metabolic rate than the freshwater one. Between 5 and 35°C Q ₁₀-values range from 4.01 to 1.37.

     

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.

     

Field and Experimental Studies on the Effects of a power station effluent on tubificidae (Oligochaeta,Annelida)

1. Higher numbers of sexually mature worms of L. hoffmeisteri were found in the River Trent downstream from Drakelow Power Stations than upstream.
2. The condenser effluent from the power stations not only increased the temperature of the river but also produced a considerable increase in the concentration of dissolved oxygen.
3. Experiments were therefore carried out on the effects of these two variables on the reproductive rate of the worms.
4. In these experiments it was found that: (a) L. hoffmeisteri increased its rate of egg production with increase in temperature up to about 25°C while T. tubifex maintained a fairly steady rate of egg production over a range of temperatures from 10–25°C. (b) L. hoffmeisteri maintained a fairly steady rate of egg and cocoon production over a wide range of oxygen concentrations above 2 ppm.
5. Therefore it seems likely that the difference between the numbers of sexually mature L. hoffmeisteri upstream and downstream from the power station were influenced more by the increased temperature, than the increased oxygen levels of the power station effluent, though under extreme conditions of deoxygenation, aeration of the river by the cooling towers at the power stations could increase the abundance of this species.

     

Metabolic responses of the mussels Perna viridis and Perna indica to declining oxygen tension at different salinities

• 1.1. Oxygen uptake and ammonia loss were monitored during responses to reductions of both salinity and oxygen tension (PO₂) in the marine mussels Perna viridis and Perna indica from southern India.
• 2.2. The proportional contribution of protein to total catabolic substrates under natural environmental conditions was as much as 96% in P. viridis, relative to only 19% in P. indica.
• 3.3. Normoxic oxygen consumption remained statistically unchanged in P. viridis conditioned to salinities between 32 and 15‰, with no obvious signs of distress. Although equally unaffected at salinities between 32 and 20‰, P. indica showed significantly reduced oxygen uptake following transfer from 32 to 15‰, and had died within the next 7 days.
• 4.4. At salinities greater than 20‰, P. viridis was better able than P. indica to regulate oxygen consumption independent of PO₂.
• 5.5. P. indica showed a compensatory increase in oxyregulatory capacity at 15‰. This exceeded unstressed abilities, helping to maintain albeit reduced oxygen uptake throughout wider ranges of PO₂.
• 6.6. Different responses recorded in each of these tropical and often intertidal species were in accordance with their natural distributions. Nevertheless, the oxyregulatory capacity in both species was higher than in bivalves from temperate and/or subtidally restricted habitats.

     

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.

     

Diurnal variation in Sagar Lake,Sagar (India) I studies in the deep water area

1. A diurnal study of inland fresh water lake has been made with respect to physical and chemical properties and the plankton.
2. Chlorides have followed the total carbonates while dissolved oxygen and pH have shown no relation.
3. Microcystis has followed no definite pattern of diurnal movement.
4. All crustaceans, some of the rotifers andTrachelomonas perform considerable diurnal movement in the course of a twenty four hour period.

     

Effect of feeding on the respiration rate of the rotifer Brachionus plicatilis

The effect of feeding on the respiration rate of Brachionus plicatilis was studied. Oxygen consumption was determined under two feeding regimes, duplicate feeding and constant feeding. Oxygen consumption rate increased during feeding. The oxygen consumption profile is discussed in relation to the following processes:

1. filtration, mastication, and locomotion during feeding
2. specific dynamic action (SDA)
3. egg formation and routine metabolism.

     

The effect of inspired oxygen tension on oxygen uptake and tolerance to anoxia in the water snakes Helicops modestus and Liophis miliaris (Colubridae)

• 1.1. The effect of oxygen tension, p_o2, on oxygen uptake and tolerance to anoxia have been studied by exposure in nitrogen atmosphere and diving in the water snakes Helicops modestus and Liophis miliaris, at 25°C.
• 2.2. The critical P_o2, was the same (70mmHg O₂) for both species, but below that tension H. modestus showed a higher degree of dependence on P_o2.
• 3.3. Anoxia tolerance time was longer (14 min for H. modestus and 4 min for L. miliaris) during forced dive than during exposure to a 100% nitrogen atmosphere. No difference was found in pre- and post-forced dive oxygen uptake values in both species.
• 4.4. The maximum duration of a voluntary dive was shorter than the mean tolerance time to forced dives in L. miliaris. but longer in H. modestus.
• 5.5. H. modestus, the more aquatic species, is significantly more tolerant of complete anoxia (100% N₂ exposure) and submersion.

     

Temperature acclimatization in the filtering rates and oxygen consumption of Daphnia ambigua scourfield

• 1.1. Filtering rates and oxygen consumption were measured in the field on a wild population of the fresh-water limnetic cladoceran Daphnia ambigua.
• 2.2. Filtering rates increased with increasing body size and were significantly affected by environmental temperature.
• 3.3. Oxygen consumption increased with increasing body size; there was no significant difference among b values determined at different environmental temperatures but bs were highest at low temperatures. decreased progressively at higher temperatures and increased at the highest temperatures.
• 4.4. Temperature significantly affected the rate of oxygen consumption.
• 5.5. Both filtering rates and oxygen consumption evidenced classical translation to the left in cold-acclimatized animals. An environmental temperature near 12°C apparently separates warm- and cold-acclimatization processes.

     

Oxygen consumption in the fathead minnow (Pimephales promelas rafinesque)-I: Effects of weight,temperature, group size,oxygen level and opercular movement rate as a function of temperature1

• 1.1. A relationship is evident between oxygen consumption (OC in cm³/hr) and weight (WT in g) such that: OC = −0.580 (WT)^1.053
• 2.2. Fathead minnows failed to exhibit immediate rate compensation as a result of acute temperature changes. Minnows showed an exponential increase in weight-specific oxygen consumption with temperature (in °C), resulting in a Q₁₀ of over three. The equation is: OC = 10^0.0482 (Temp.) − 1.268.
• 3.3. Minnows acclimated to water temperatures of 5–21°C showed a steady increase in opercular movement rates (OMR) (ventilation rates) as expressed by the equation: OMR = 0.1968 (Temp.)² + 1.064.
• 4.4. Grouping more than two fish per chamber resulted in an increase in oxygen consumption. The relationship of group size (GS) to oxygen consumption is: OC = 0.04059 (GS)² − 0.2017 (GS) + 0.5353.
• 5.5. Oxygen consumption is a function of dissolved oxygen level. This relationship is shown by the equation: OC = 0.003049 (OL)³ − 0.06359 (OL)² + 0.4211 (OL) − 0.4020 where OL is oxygen level. Due to high variability, it is statistically impossible to determine oxygen level ranges in which they conformed and those in which they regulated.

     

Skeleton weight-free oxygen consumption related to adaptations to environment and habits of six crustacean species

• 1.1. Oxygen consumption in six crustacean species from the continental shelf of the NW Gulf of Mexico was related to the ash free weight per dry weight (afdw) gram of the tissue excluding the exoskeleton, suggesting a close relationship to their life strategies.
• 2.2. Dry weight exoskeleton proportion varied among species, with highest values recorded in callapid brachyuran crab species (46.8–52.5%) against the values recorded in portunid crab (45.8–48%) and the shrimp species (26.7–35.7%).
• 3.3. Oxygen consumption was related to afdw in each species according to the expression y = ax^b, with b values ranging from 0.68 to 2.92.
• 4.4. Rates of oxygen consumption per afdw/dw were larger in shrimps than in portunids and callapids, and was related to the morphophysiology and lifestyle of six species described; the former as the morphological design of the exoskeleton versus the muscle content in the species and the latter as the activity rate in the environment.
• 5.5. The oxygen extraction efficiency, calculated from oxygen consumption, was higher in the eurytopic species Penaeus aztecus and Callinecies similis than in species restricted to the marine environment, hence considered as a response to environmental fluctuations.