scholarly journals The Relative Efficiency of Gaseous Exchange Across the Lungs and Gills of an African Lungfish Protopterus Aethiopicus

1970 ◽  
Vol 52 (1) ◽  
pp. 1-15
Author(s):  
B. R. McMAHON

1. The efficiency of gas exchange over the lung and gill surfaces of Protopterus has been investigated. 2. Animals confined in water or in air showed an increased respiratory frequency in the remaining medium, indicating that both routes were important in the total gas exchange. 3. Direct measurement of the oxygen and carbon dioxide tensions of pulmonary air and inspired and expired branchial water showed gas exchange ratios (R) of 0.2 for the lung and 5.0 for the gills approximately, demonstrating that more oxygen was consumed via the lungs and more carbon dioxide excreted via the gills. 4. Oxygen consumption and carbon dioxide production were measured directly in a respirometer in which respiratory air and water streams could be kept separate except during lung ventilation. At least 90% of the animals' oxygen consumption occurred in the lung, while 60 % of the carbon dioxide excreted passed via the aquatic route. 5. The results are discussed with reference to the animals' adaptation to its environment and with reference to the evolution of the terrestrial vertebrates.

1998 ◽  
Vol 84 (6) ◽  
pp. 2177-2182 ◽  
Author(s):  
Saul Miodownik ◽  
Jose Melendez ◽  
Vittoria Arslan Carlon ◽  
Brian Burda

The methanol-burning lung model has been used as a technique for generating a predictable ratio of carbon dioxide production (V˙co 2) to oxygen consumption (V˙o 2) or respiratory quotient (RQ). Although an accurate RQ can be generated, quantitatively predictable and adjustableV˙o 2 andV˙co 2 cannot be generated. We describe a new burner device in which the combustion rate of methanol is always equal to the infusion rate of fuel over an extended range of O2 concentrations. This permits the assembly of a methanol-burning lung model that is usable with O2 concentrations up to 100% and provides continuously adjustable and quantitativeV˙o 2 (69–1,525 ml/min) and V˙co 2 (46–1,016 ml/min) at a RQ of 0.667.


Author(s):  
Willie J. Van Aardt ◽  
Japie Mienie ◽  
J.M. Le Roux

Adult scorpions (2.4g – 4.5 kg) were collected near Potchefstroom (26° .55’10” – 27° 10” 5”). Oxygen consumption rate (MO2) and carbon dioxide production rate (MCO2) were measured together with the metabolism of injected radioactive glucose.


1979 ◽  
Vol 57 (6) ◽  
pp. 615-618 ◽  
Author(s):  
H. Green ◽  
M. Houston ◽  
J. Thomson ◽  
P. Reid

The relationships between ventilation [Formula: see text], oxygen consumption [Formula: see text], and carbon dioxide production [Formula: see text] during work were studied in four trained males during exercise-induced carbohydrate depletion. Repeated bouts of heavy treadmill exercise (6 min at 95% [Formula: see text]max) were performed once per hour for 24 h in order to promote a shift in energy substrate from carbohydrate to fat. Measurements of [Formula: see text] and [Formula: see text] recorded during each minute indicated that [Formula: see text] was unaffected by the number of runs, whereas [Formula: see text] showed a progressive reduction which amounted to 24% during the final run. A corresponding decline of 19% was observed in the respiratory exchange ratio. No significant change in [Formula: see text] occurred between any of the runs. It is concluded that during heavy, repeated, muscular exercise, reductions in [Formula: see text], strongly suggestive of an increased fat oxidation, are not accompanied by a corresponding change in ventilation.


1992 ◽  
Vol 70 (3) ◽  
pp. 408-411 ◽  
Author(s):  
Peter B. Frappell ◽  
Andrea Dotta ◽  
Jacopo P. Mortola

Aerobic metabolism (oxygen consumption, [Formula: see text], and carbon dioxide production, [Formula: see text]) has been measured in newborn rats at 2 days of age during normoxia, 30 min of hyperoxia (100% O2) and an additional 30 min of recovery in normoxia at ambient temperatures of 35 °C (thermoneutrality) or 30 °C. In normoxia, at 30 °C [Formula: see text] was higher than at 35 °C. With hyperoxia, [Formula: see text] increased in all cases, but more so at 30 °C (+20%) than at 35 °C (+9%). Upon return to normoxia, metabolism readily returned to the prehyperoxic value. The results support the concept that the normoxic metabolic rate of the newborn can be limited by the availability of oxygen. At temperatures below thermoneutrality the higher metabolic needs aggravate the limitation in oxygen availability, and the positive effects of hyperoxia on [Formula: see text] are therefore more apparent.Key words: neonatal respiration, oxygen consumption, thermoregulation.


PEDIATRICS ◽  
1964 ◽  
Vol 33 (1) ◽  
pp. 75-82
Author(s):  
Forrest H. Adams ◽  
Tetsuro Fujiwara ◽  
Robert Spears ◽  
Joan Hodgman

Thirty-four measurements of oxygen consumption, carbon dioxide production, respiratory quotient, and rectal temperature were made on 22 premature infants with ages ranging from 2½ hours to 18 days. The studies were conducted at 32-34°C utilizing an open circuit apparatus and a specially designed climatized chamber. Oxygen consumption and carbon dioxide production were lowest in the first 12 hours and increased thereafter. The rate of increase in O2 consumption was greater than that of CO2 production, with a consequent fall in respiratory quotient during the first 76 hours of life. A reverse relation of O2 consumption and CO2 production was found following the 4th day of life with a consequent rise in respiratory quotient. There was a close correlation between O2 consumption and rectal temperature regardless of age. A respiratory quotient below the value of 0.707 for fat metabolism was observed in 7 premature infants with ages ranging from 24 to 76 hours.


1958 ◽  
Vol 193 (3) ◽  
pp. 495-498 ◽  
Author(s):  
Ruth McClintock ◽  
Nathan Lifson

Measurements of oxygen consumption and carbon dioxide production were made by the Haldane open circuit method on hereditarily obese mice and littermate controls, and the energy expenditures were estimated. Studies were made on mice for short periods under ‘basal’ conditions, and for periods of approximately a day with the mice fasted and confined, fasted and relatively unconfined, and fed and unconfined. The total energy expenditures of fed and unconfined obese mice were found to be higher than those of nonobese littermate controls by virtue of a) increased ‘basal metabolism’, b) greater energy expenditure associated with feeding, and possibly c) larger energy output for activity despite reduced voluntary movement. The values obtained for total metabolism confirm those previously determined by an isotope method for measuring CO2 output.


2018 ◽  
pp. 94-100
Author(s):  
John R. B. Lighton

This chapter demystifies respirometry equations, showing how they can be derived using a simple mental trick: focusing the analysis on the principal gas that is neither consumed nor produced by animals. The effect of dilution of oxygen by carbon dioxide, the enrichment of carbon dioxide by the consumption of oxygen, and the effects of water vapor on the concentrations of both gases are described and quantified. A system of eight equations is derived that allow oxygen consumption and carbon dioxide production to be calculated in practically any feasible flow-through respirometry system.


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