THE RESPIRATORY QUOTIENT OF FROG NERVE DURING STIMULATION

1. By means of a differential volumeter the increased oxygen consumption and the increased carbon dioxide output of frog nerve during and after stimulation have been observed. 2. Measurements of the R.Q. of nerve by this method are complicated by the retention of carbon dioxide. Attempts were made to avoid this (a) by studying the nerves at high CO₂ tensions to make the retention small and (b) by calculating the amount of CO₂ retained from the carbon dioxide dissociation curve of nerve and applying this value as a correction. 3. The results of both those methods when averaged together give an R.Q. of the excess metabolism of 1.19 and an R.Q. of the resting nerve of 0.97. 4. Observations on the time course of the gas exchange during stimulation indicate a delay in the appearance of the extra carbon dioxide output relative to the oxygen intake. 5. Very similar time curves can be calculated from the diffusion coefficients and the solubilities of the oxygen and the carbon dioxide.     

A Mathematical Model of the Controlled Plant of the Réspiratory System

Ability to predict the dynamic response of oxygen, carbon dioxide tensions, and pH in blood and tissues to abrupt changes in ventilation is important in the mathematical modeling of the respiratory system. In this study, the controlled plant (the amount and distribution of O₂ and CO₂) of the respiratory system is modeled. Although the body tissues are divided into a finite number of “compartments” (three tissue groups), in contrast to earlier models, the blood and tissue gas tensions within each compartment are considered to be continuously distributed in time and in one spatial coordinate. The mass conservation equations for oxygen and carbon dioxide involved in the blood-tissue gas exchange are described by a set of partial differential equations which take into account convection of O₂ and CO₂ caused by the flow of blood as well as diffusion due to local tension gradients. Nonlinear algebraic equations for the dissociation curves, which take into account the Haldane and Bohr effects in blood, are used to obtain the relationships between concentrations and partial pressures. Time-variable delays caused by the arterial and venous transport of the respiratory gases are also included. The model so constructed successfully reproduced actual O₂ and CO₂ tensions in arterial blood, and in muscle venous and mixed venous blood when ventilation was abruptly changed.     

THE DIFFUSION OF CARBON DIOXIDE IN TISSUES

1. Two methods are given for measuring the rate of diffusion of CO₂ in tissue membranes. Methods are also given for the determination of tissue thickness and the absorption coefficient for CO₂ in tissues. 2. The values obtained for the permeability constant (P x 10⁴) at 22°C. for CO₂ in the following tissues are:—frog skin, 3.05; connective tissue (dog), 2.65; smooth muscle (cat), 5.00; frog muscle, 5.29; striated muscle (dog), 4.70. P is expressed as cc. per cm.² per minute under a pressure gradient of one atmosphere per cm. 3. Evidence is presented to show that in a "steady state" bicarbonate contributes a negligible amount to the diffusion of CO₂. 4. The absorption coefficient for CO₂ in frog skin is 0.73 cc. per cc. and for frog muscle 0.78 cc. per cc. 5. In all of the tissues studied the diffusion of CO₂ is slower than in water. The diffusion coefficients (K x 10⁴ in cm.²/minute) at 22°C. for tissues as compared with water are:—water (16°C.), 9.5 (Hüfner, 1897); frog skin, 4.1; connective tissue, 3.7; frog muscle, 6.8; striated muscle (dog), 6.0; smooth muscle (cat), 6.4. 6. The time course of saturation of a tissue with CO₂ is altered in the presence of available base. Non-acidified tissues saturate more slowly than acidified tissues and the rate of saturation is dependent on the CO₂ tension.     

DYNAMICS OF NERVE CELLS : II. THE TEMPERATURE COEFFICIENTS OF CARBON DIOXIDE PRODUCTION BY THE HEART GANGLION OF LIMULUS POLYPHEMUS.

1. It is possible to determine by the colorimetric method the rate of production of carbon dioxide by the cardiac ganglion of Limulus. 2. Carbon dioxide formation in the cardiac ganglion was found to run parallel to the rate of heart beat for different temperatures. 3. The conclusion seems justified that the rate of cardiac rhythm of Limulus depends upon a chemical reaction in the nerve cells of the cardiac ganglion and that this reaction is associated with the production of carbon dioxide since the rate of beat and the rate of CO₂ production are similarly affected by changes in temperature.     

THE EFFECTS OF OXYGEN,CARBON DIOXIDE,AND PRESSURE ON GROWTH IN CHILOMONAS PARAMECIUM AND TETRAHYMENA GELEII FURGASON

1. The effects of O₂, CO₂, and pressure were studied in two very different species of protozoa, a flagellate, Chilomonas paramecium, grown in acetate-ammonium solution and a ciliate, Tetrahymena geleii, grown in 2 per cent proteose-peptone solution. 2. Chilomonas and Tetrahymena live and reproduce in solutions exposed to a wide range of O₂ concentrations, but Chilomonas is killed at high O₂ tensions in which Tetrahymena grows best. The optimum O₂ concentration for Chilomonas is about 75 mm. pressure but it lives and reproduces in O₂ tensions as low as 0.5 mm. while Tetrahymena fails to grow in concentrations below 10 mm. O₂ pressure. 3. With a constant O₂ tension of 50 mm. pressure, it was found that there is no significant variation in growth in Chilomonas between 50 mm. and 740 mm. total pressure. In Tetrahymena, however, under the same conditions, an optimum total pressure was found at about 500 mm. and growth is comparatively poor at 50 mm. total pressure. 4. Tetrahymena does not live very long in CO₂ tensions over 122 mm., although Chilomonas grows as well at 400 mm. CO₂ as in air at atmospheric pressure (0.2 mm. CO₂). Tetrahymena grows best in an environment minus CO₂, but the optimum for Chilomonas is 100 mm. CO₂ at which pressure an average of 668,600 ± 30,000 organisms per ml. was produced (temperature, 25 ± 1° C.). 5. Chilomonads grown in high CO₂ concentrations (e.g., 122 mm.) produce larger starch granules and more starch than those grown in ordinary air at atmospheric pressure. 6. In solutions exposed to 75 mm. O₂ tension (optimum) and 122 mm. CO₂ plus 540 mm. N₂ pressure, chilomonads contain very little, if any, fat. This phenomenon seems to be due to the action of CO₂ on the mechanisms concerned with fat production. 7. In Tetrahymena exposed to pure O₂, there is very little fat compared to those grown in atmospheric air. This may be due to the greater oxidation of fat in the higher O₂ concentrations. 8. Further evidence is presented in support of the contention that Chilomonas utilizes CO₂ in the production of starch.     

Respiratory properties of the blood of the burrowing red band fish Cepola rubescens L.

The respiratory properties of the whole blood of the burrowing red band fish Cepola rubescens L. were investigated. Oxygen dissociation curves constructed at 15°C were found to be close to hyperbolic in shape with a mean value for the cooperativity coefficient at half-saturation (n₅₀) of 1.56. Half-saturation oxygen tension (P₅₀) for pH = 7.56 (mean in vivo pH of venous blood) was 27 Torr. The blood showed a marked Bohr effect ($\text{Δ log}\text{P}{}_{50}\text{ΔpH}\text{= ?1.19}$) and also a Root effect which at the in vivo pH reduced oxygen carrying capacity by 20%. The Pv_CO2 was 3.2 Torr and the buffering power of the blood was low, the buffer value of true plasma averaging 5.43 mmol · 1^?1 · pH^?1. It is suggested that the large Bohr effect coupled with the low buffer value confers on the haemoglobin a flexibility, in terms of oxygen affinity, to withstand changes which occur in environmental oxygen tensions.     

Pre-and post-branchial blood respiratory status during acute hypercapnia or hypoxia in rainbow trout,Oncorhynchus mykiss

Simultaneous venous (pre-branchial) and arterial (post-branchial) extracorporeal blood circulations were utilized to monitor continuously the rapid and progressive effects of acute environmental hypercapnia (water partial pressure of CO₂ 4.8±0.2 torr) or hypoxia (water partial pressure of O₂ 25±2 torr) on oxygen and carbon dioxide tensions and pH in the blood of rainbow trout (Oncorhynchus mykiss). During hypercapnia, the CO₂ tension in the arterial blood increased from 1.7±0.1 to 6.2±0.2 torr within 20 min and this was associated with a decrease of arterial extracellular pH from 7.95±0.03 to 7.38±0.03; the acid-base status of the mixed venous blood changed in a similar fashion. The decrease in blood pH in vivo was greater than in blood equilibrated in vitro with a similar CO₂ tension indicating a significant metabolic component to the acidosis in vivo. Under normocapnic conditions, venous blood CO₂ tension was slightly higher than arterial blood CO₂ tension difference was abolished or reversed during the initial 25 min of hypercapnia indicating that CO₂ was absorbed from the water during this period. Arterial O₂ tension remained constant during hypercapnia; however, venous blood O₂ tension decreased significantly (from 22.0±2.6 to 9.0±1.0 torr) during the initial 10 min. Hypercapnia elicited the release of catecholamines (adrenaline and noradrenaline) into the blood. The adrenaline concentration increased from 6±3 to 418±141 nmol · l^-1 within 25 min; noradrenaline concentration increased from 3±0.5 to 50±21 nmol · l^-1 within 15 min. During hypoxia arterial blood O₂ tension declined progressively from 108.4±9.9 to 12.8±1.7 torr within 30 min. Venous blood O₂ tension initially was stable but then decreased abruptly as catecholamines were released into the circulation. The release of catecholamines occurred concomitantly with a sudden metabolic acidosis in both blood compartments and a rise in CO₂ tension in the mixed venous blood only.Abbreviations CCO₂ plasmatotal carbondioxide - CtO₂ blood oxygen content - PO₂ partial pressure of oxygen - PCO₂ partial pressure of carbon dioxide - PaO₂ arterial bloodPO₂ - PaCO₂ arterial bloodPCO₂ - PvCO₂ venous bloodPCO₂ - PwO₂ waterPO₂ - PwCO₂ waterPCO₂ - Hb haemoglobin - SHbO₂ haemoglobin oxygen saturation - HPLC high-performance liquid chromatography - rbc red blood cell(s) - Hct haematocrit     

Algorithm for computing oxygen dissociation curve with pH,PCO2, and CO in sheep blood

By extending the study of Samaja and Gattinoni¹, an algorithm is described for computing the oxygen dissociation curve with variations in pH, PCO₂, and CO in homozygous HbB sheep blood. The difference in the values of O₂ pressure at 50% saturation in presence of CO computed from the present algorithm and Hill's equation does not exceed 0.5%. It is shown that O₂ affinity increases as the concentration of CO or pH increases or PCO₂ decreases. The algorithm is convenient for representing the oxygen dissociation curve with variation in pH, PCO₂ and the concentration of CO in modelling oxygen transport in sheep blood even under hypoxic conditions.     

Enhancement of carbon dioxide fixation by alteration of illumination duringChlorella vulgaris-Buitenzorg's growth

Alteration of illumination with optimum carbon dioxide fixation-based curve in this research successfully enhanced the CO₂-fixation (q_co2) capability ofChlorella vulgaris Buitenzorg cultivated in a bubble column photo bioreactor. The level of CO₂ fixation was up to 1.91 times that observed from cultivation with intensification of illumination on an optimum growth-based curve. During 144 h of cultivation, alteration of light intensity on an optimum CO₂-fixation-based curve produced a q_CO2 of 6.68 h^?1. Increases in light intensity based on a curve of optimum CO₂-fixation produced a final cell concentration of about 5.78 g/L. Both cultivation methods were carried out under ambient pressure at a temperature of 29°C with a superficial gas velocity of 2.4 m/h (U_G). Cells were grown on Beneck medium in a 1.0 L Bubble Column Photo bioreactor illuminated by aPhillips Halogen Lamp (20 W/12 V/50 Hz). The inlet gas had a carbon dioxide content of 10%.     

THE EFFECT OF CARBON DIOXIDE TENSION ON THE METABOLISM OF CEREBRAL CORTEX AND MEDULLA OBLONGATA

Manometric measurements were made of oxygen uptake (Q _OO2) and aerobic lactic acid output (Q_G) by slices of cerebral cortex and medulla oblongata of the cat in the presence of mixtures of 1, 5, and 20 volumes per cent of carbon dioxide in oxygen. The concentrations of NaHCO₃ and NaCl in the medium were varied to maintain constant pH and sodium ion concentrations. The calcium ion concentration was 0.0002 M. At pH 7.5 under these conditions, an increase in carbon dioxide from 1 per cent to 5 per cent doubled the Q_G of both tissues but did not alter Q _OO2; an increase from 5 per cent to 20 per cent carbon dioxide had no further effect on Q_G in either tissue or Q _OO2 of cortex, but did depress the Q _OO2 of medulla. At pH 8.1, an increase in carbon dioxide from 1 per cent to 5 per cent raised the Q _OO2 and Q_G of cortex by about 60 per cent. Measurements at low oxygen tension carried out previously in phosphate medium were repeated in bicarbonate medium to obtain data for the combined output of lactic acid and carbon dioxide (Q_A). When the oxygen in the gas phase was decreased from 95 to 3 volumes per cent, the lactic acid output as measured colorimetrically increased by 114 mg./gm. in cortex and by 8 mg./gm. in medulla; Q_A increased from 12.3 to 13.5 in cortex and decreased from 5.1 to 3.8 in medulla.     

ENHANCED TRANSPORT OF INORGANIC CARBON INTO ALGAL CELLS AND ITS IMPLICATIONS FOR THE BIOLOGICAL FIXATION OF CARBON1,2

Kinetics of uptake of inorganic carbon by the freshwater green alga Chlamydomonas reinhardtii Dang. suggest that rates of fixation may be enhanced at low tensions of CO₂ by transport of bicarbonate from the cell surface to the chloroplast. Results are evaluated in the context of models that treat diffusion and reaction of dissolved inorganic carbon across a 3 dimensional finite boundary layer, and they are consistent with the claim that CO₂ alone is the substrate used during carbon fixation. An alternative hypothesis, which presumes that both CO₂ and bicarbonate are used as substrates, yields predictions which are inconsistent with the data. Instead, bicarbonate seems to act only as a vehicle for the transport of inorganic carbon into the cell, thereby adding its flux to that of CO₂, and enhancing rates of synthesis that would otherwise be restricted by uptake of CO₂ alone.     

ON THE GROWTH AND RESPIRATION OF SULFUR-OXIDIZING BACTERIA

1. It is shown that Sulfomonas thiooxidans oxidizes elementary sulfur completely to sulfuric acid. Sodium thiosulfate is oxidized by this organism completely to sulfate. Sulfomonas thiooxidans differs, in this respect, from various other sulfur-oxidizing bacilli which either produce elementary sulfur, from the thiosulfate, or convert it into sulfates and persulfates. 2. The organism derives its carbon from the CO₂ of the atmosphere, but is incapable of deriving the carbon from carbonates or organic matter. 3. The S:C, or ratio between the amount of sulfur oxidized to sulfate and amount of carbon assimilated chemosynthetically from the CO₂ of the atmosphere, is, with elementary sulfur as a source of energy, 31.8, and with thiosulfate 64.2. The higher ratio in the case of the thiosulfate is due to the smaller amount of energy liberated in the oxidation of sulfur compound than in the elementary form. 4. Of the total energy made available in the oxidation of the sulfur to sulfuric acid, only 6.65 per cent is used by the organism for the reduction of atmospheric CO₂ and assimilation of carbon. 5. Sulfates do not exert any injurious effect upon sulfur oxidation by Sulfomonas thiooxidans. Any effect obtained is due to the cation rather than the sulfate radical. Nitrates exert a distinctly injurious action both on the growth and respiration of the organism. 6. There is a definite correlation between the amount of sulfur present and velocity of oxidation, very similar to that found in the growth of yeasts and nitrifying bacteria. Oxidation reaches a maximum with about 25 gm. of sulfur added to 100 cc. of medium. However, larger amounts of sulfur have no injurious effect. 7. Dextrose does not exert any appreciable injurious effect in concentrations less than 5 per cent. The injurious effect of peptone sets in at 0.1 per cent concentration and brings sulfur oxidation almost to a standstill in 1 per cent concentration. Dextrose does not exert any appreciable influence upon sulfur oxidation and carbon assimilation from the carbon dioxide of the atmosphere. 8. Sulfomonas thiooxidans can withstand large concentrations of sulfuric acid. The oxidation of sulfur is affected only to a small extent even by 0.25 molar initial concentration of the acid. In 0.5 molar solutions, the injurious effect becomes marked. The organism may produce as much as 1.5 molar acid, without being destroyed. 9. Growth is at an optimum at a hydrogen ion concentration equivalent to pH 2.0 to 5.5, dropping down rapidly on the alkaline side, but not to such an extent on the acid, particularly when a pure culture is employed. 10. Respiration of the sulfur-oxidizing bacteria can be studied by using the filtrate of a vigorously growing culture, to which a definite amount of sulfur is added, and incubating for 12 to 24 hours.     

REDUCTION OF CARBON DIOXIDE COUPLED WITH THE OXYHYDROGEN REACTION IN ALGAE

1. Unicellular algae possessing a hydrogenase system (Scenedesmus and other species), and having been adapted by anaerobic incubation to the hydrogen metabolism, reduce oxygen to water according to the equation O₂ + 2H₂ → 2H₂O. 2. The oxyhydrogen reaction proceeds undisturbed only in the presence of carbon dioxide, which simultaneously is reduced according to the equation CO₂ + 2H₂ → H₂O + (CH₂O) = (carbohydrate). 3. The maximum yield of the induced reduction is one-half molecule of carbon dioxide reduced for each molecule of oxygen absorbed. 4. Partial reactions are recognizable in the course of the formation of water and it is with the absorption of the second equivalent of hydrogen that the carbon dioxide reduction appears to be coupled. 5. The velocity of the reaction increases in proportion to the partial pressure of oxygen, but only up to a certain point where any excess of oxygen causes the inactivation of the hydrogenase system. The reaction then ends prematurely. 6. During the oxyhydrogen reaction little or no oxygen is consumed for normal respiratory processes. 7. Small concentrations of cyanide, affecting neither photosynthesis nor photoreduction in the same cells, first inhibit the induced reduction of carbon dioxide and then lead to a complete inactivation of the hydrogenase system. 8. Hydroxylamine, added after adaptation, has either no inhibitory effect at all, or prevents solely the induced reduction of carbon dioxide without inactivating the hydrogenase system. 9. Dinitrophenol prevents the dark reduction of carbon dioxide while the reduction of oxygen continues to the formation of water. 10. Glucose diminishes the absorption of hydrogen, probably in its capacity as a competing hydrogen donor. 11. The induced reduction of carbon dioxide can be described as an oxido-reduction similar to that produced photochemically in the same cells.     

Gas exchange and air flow in the lung of the snake,Pituophis melanoleucus

Summary Gas samples from various regions of the lung were obtained throughout the breathing cycle inPituophis melanoleucus. Changes in CO₂ concentration during the interbreath period differed markedly along the length of the lung. In general, the largest and most rapid increases in CO₂ tension were measured at the cranial end of the vascular lung. Further caudad in the vascular lung, the increase was slower and did not reach mixed venous CO₂ tension before exhalation. In animals exhibiting the lowest breathing frequencies and presumably larger tidal volumes, the region of gas exchange extended into the cranial portion of the air sac. There was little or no change in gas tensions within the remaining caudal regions of the air sac. Measurement of exhaled CO₂ and O₂ tensions at the nares confirmed the longitudinal gradient in gas exchange and also demonstrated the sequential emptying of the lung. Large regional differences in the ratio of blood flow to alveolar volume are probably responsible for the gradients in lung gases.Interpretation of N₂ clearance curves in terms of two freely communicating compartments demonstrated the presence of a ventilation inequality. Consistent with this was the lack of body wall contractions between breaths while animals were resting. However, just prior to and during activity body wall contractions not associated with breathing often occurred and resulted in pressure excursions in the lung of ca. five mm H₂O. In addition, the heart beat results in a pressure change within the lung of ca. 0.2 mmH₂O which may be significant in gas mixing.     

Studies on the Ventilation in Submerged Fermentations

Quantitative studies on the dissolution and dissociation of carbon dioxide in a cultured system were made. The inosine fermentation and the glutamic acid fermentation were employed for this study. According to the results obtained in this experiment, the quantity of dissociated carbonic acid in cultured liquid was given by Henderson-Hasselbalch’s equation with experimental pK′. The method for the direct determination of bicarbonate ion concentration was also investigated. The Warburg direct method gave a satisfactory result for this purpose.

By using the modified Severinghaus CO₂ electrode, the relationship between partial pressure of carbon dioxide in effluent gas and that in culturing system was investigated. Partial pressure of carbon dioxide in gas phase was almost equivalent to the average value of dissolved carbon dioxide tension in liquid phase for a given short time of the fermentation. The term of r_e was introduced in order to study the dynamic characteristics of carbon dioxide evolution in submerged fermentors. The dynamic characteristics of respiration in submerged fermentation was also studied by using biological r_ab and r_e.     

Photosynthetic and Stomatal Responses of the Grey Mangrove, Avicennia marina, to Transient Salinity Conditions

Measurements of gas exchange characteristics were made on intact, attached leaves of hydroponically grown seedlings of Avicennia marina (Forstk.) Vierh. var australasica (Walp.) Moldenke as the NaCl concentration of the culture solution was varied by step changes of 50 millimolar NaCl every 2nd day from 50 to 500 to 50 millimolar NaCl. The CO₂ assimilation rate, stomatal conductance, intercellular CO₂ concentration, and evaporation rate decreased at salinities above 250 millimolar NaCl and recovered substantially upon return to the original salinity.

The assimilation rate was measured as a function of the intercellular CO₂ concentration [A(c_i) curve]. The lower linear portion of this curve was insensitive to variation in salinity, whereas the upper nonlinear portion declined with increasing salinity, indicating a reduction in the capacity for CO₂ assimilation which recovered upon return to the original salinity. Stomatal conductance changed such that the intercellular CO₂ concentration measured under normal atmospheric conditions occurred in the transition between the lower, linear and upper nonlinear portions of the A(c_i) curve. Thus, stomatal conductance and photosynthetic capacity together co-limited the assimilation rate. The changes in gas exchange characteristics were such that water loss was minimal relative to carbon gain.

     

The effect of low levels of carbon dioxide on metabolism of Mus musculus

• 1.1. In this study we measured the metabolic response of individual mice to low concentrations of carbon dioxide in air (0.14 to 1.7%). Both oxygen consumption (V_o2) and carbon dioxide (V_o2) were determined, and the respiratory quotient (R) was calculated.
• 2.2. V_o2 was significantly reduced at levels of 0.14 to 0.50% CO₂ in the air. At 0.23% for example, V_o2 dropped from 3.11 ± 0.6 to 1.26 ± 0.69 cc O₂/g × hr. R increased from 0.7 to 1.0 and higher throughout the 6-hr testing period, which consisted of 1.5 hr of exposure to 0.0% CO₂, 1.5 hr of exposure to a test gas and a repetition of 1.5 hr each of baseline and test exposures.
• 3.3. We conclude that low levels of CO₂ such as mice might encounter in a nest, burrow or even metabolic chamber may effect a feedback mechanism which acts to decrease metabolism.

     

THE INFLUENCE OF HYPOCAPNIA UPON INTRACELLULAR pH AND UPON SOME CARBOHYDRATE SUBSTRATES, AMINO ACIDS AND ORGANIC PHOSPHATES IN THE BRAIN

Abstract— In order to evaluate the influence of hypocapnia upon the energy metabolism of the brain, lightly anaesthetized rats were hyperventilated to arterial CO₂ tensions of 26, 15 and 10 mm Hg respectively, with subsequent measurements of intracellular pH and of tissue concentrations of carbohydrate substrates, amino acids and organic phosphates. At P_co1= 26 there was a moderate increase in the intracellular pH but when the P_co2 was reduced further to 10 mm Hg the intracellular pH returned to normal, or slightly subnormal, values. The reduction in P_Co2 was accompanied by increased cerebral cortical concentrations of lactate, pyruvate, citrate, α-ketoglutarate, malate and glutamate and by decreased aspartate concentrations. It is concluded that the accumulation of metabolic acids explains the normal value for intracellular pH at very low CO₂ tensions. Previous results obtained in man indicate that there is an increased anaerobic production of lactic acid in the brain in extreme hypocapnia. At comparable CO₂ tensions the present results showed a small fall in phosphocreatine and a small rise in ADP. However, since the ammonia concentrations were normal or decreased and since there was an increase in citrate, the results give no direct support to the hypothesis of an activation of phosphofructokinase. Since the cerebral venous P_o2 was reduced to 20 mm Hg at an arterial CO₂ tension of 10 mm Hg the accumulation of acids was probably secondary to tissue hypoxia. However, since there was no, or only a very small, increase in the calculated cytoplasmic NADH/NAD⁺ ratio, it appears less likely that acids accumulated due to lack of NAD⁺.     

METABOLISM AS RELATED TO CHROMOSOME STRUCTURE AND THE DURATION OF LIFE

This paper presents the rates of CO₂ production for four groups of Drosophila which differ in their chromosome constitutions. The four groups have metabolic rates which correlate with the balance of their chromosomes, the balanced chromosome groups of flies producing less CO₂ than the unbalanced chromosome groups. It is concluded therefore that genic balance plays a prominent part in metabolic control. The carbon dioxide rates are related to the duration of life within these groups. The results show that qualitatively the larger the production of CO₂ per day the shorter the time which the flies are capable of living. The agreement is not exact quantitatively. Rubner''s theory postulating a limit for the energy an organism is capable of metabolizing does not hold for the six classes of flies. The data show that the theory can be at most not more than a partial truth. Cell size is found to show no direct correlation with the metabolic rates of the different fly cohorts.     

Arterial Blood Gas Tensions and pH in Acute Asthma in Childhood

Studies of the arterial blood gas tensions and pH in 21 children during 24 acute attacks of asthma showed that all were hypoxic on admission to hospital, and in 10 there was evidence of carbon dioxide retention. Cyanosis, invariably present when the So₂ was below 85%, and restlessness in patients breathing air were the most reliable indices of the severity of hypoxia. There were no reliable clinical guides to the Pco₂ level. Conventional oxygen therapy in tents (25–40%) did not always relieve hypoxia, and in three cases the administration of oxygen at a concentration of 40% or over failed to produce a normal arterial oxygen tension. Uncontrolled oxygen therapy may aggravate respiratory acidosis, and three of our patients developed carbon dioxide narcosis while breathing oxygen. The necessity for blood gas measurements in the management of severe acute asthma in childhood is emphasized.