Simultaneous Measurement of Oxygen, Carbon Dioxide, and Water Vapour Exchange in Intact Plants

A low flow of air is passed through a temperature-controlledplant chamber in order to obtain relatively large (300–500µl-1) differences in [O₂] between influx and efflux streams.These differences are measured with a stabilized O₂ electrodesystem incorporating elements of gas conditioning electroniczero suppression and signal amplification. Changes in [O₂] of400 µl l-1 can be detected at full scale recorder deflectionagainst a background concentration of 21% O₂. The concentrationsof CO₂ and H₂O within the chamber are held constant by con-trolled-flowCO₂-scrubbing and dehumidifying loops. Carbon dioxide, H₂O,and O₂ fluxes are measured and leaf diffusion resistance andinternal [CO₂] are calculated in essentially ‘real time’.     

The alteration of intracellular enzymes. II. The relation between the surface and the biological activities of altering agents

1. The ability of homologous series of alcohols, ketones, and aldehydes to cause alteration of intracellular catalase increases approximately threefold for each methylene group added, thus following Traube's rule. Equiactive concentrations of alcohols (methanol to octanol) varied over a 4,000-fold range, yet the average corresponding surface tension was 42 ± 2 dynes/cm., that for ketones 43 ± 2, and for aldehydes (above C₁) 41 ± 3. 2. Above C₈ the altering activity of alcohols ceased to follow Traube's rule, and at C₁₈ was nil. Yet the surface activities of alcohols from nonanol to dodecanol did follow Traube's rule. These two facts show that the interface which is being affected by these agents is not the cell surface, for if it were, altering activity should not fall off between C₉ and C₁₂ where surface activity is undiminished; they show also that micelle formation by short range association of hydrocarbon "tails," usually invoked to explain decrease in biological activity of compounds above C₈, is not responsible for this effect in these experiments, in which permeability of the cell membrane probably is involved. 3. The most soluble alcohols and aldehydes (alcohols C₁ to C₈; aldehydes C₁, C₂), but not ketones, cause, above optimal concentration, an irreversible inhibition of yeast catalase. 4. The critical concentration of altering agent (i.e., that concentration just sufficient to cause doubling of the catalase activity of the yeast suspension) was independent of the concentration of the yeast cells. 5. Viability studies show that the number of yeast cells killed by the altering agents was not related to the degree of activation of the catalase produced. While all the cells were invariably killed by concentrations of altering agent which produced complete activation, all the cells had been killed by concentrations which were insufficient to cause more than 50 per cent maximal activation. Further, the evidence suggested that the catalase may be partially activated by concentrations of altering agent which cause no decrease in viability at all. Hence alteration, unlike death, may not be all-or-none per cell. 6. The fact that the biological criterion being examined was the activation of a water-soluble enzyme rules out the possibility that the reason for the logarithmic increase in altering activity with chain length was increase in concentration of the altering agent in some intracellular fat phase. It is concluded that these surface-active agents cause enzyme alteration by becoming adsorbed at some intracellular interface and thus causing, directly or indirectly, the modification of catalase properties. 7. It is considered that these data support, but do not provide critical proof for, the interfacial hypothesis, which states that catalase is present at the intracellular interface in question, but is desorbed into solution as a consequence of the alteration process.     

Resolution of Net Dark Fixation of Carbon Dioxide into Its Respiration and Gross Fixation Components in Bryophyllum daigremontianum

Dark respiration rate increased with temperature between 10and 24°C (Q₁₀ =2.3–2.7). The rate of gross dark CO₂fixation (GDF) was affected by temperature, but irregularly.Cumulative GDF was not affected by temperature in this range.Cumulative respiration increased from 17 per cent of cumulativeGDF at 10°C, to 72 per cent at 24°C and was thus responsiblefor the 65 per cent drop in net dark fixation between thesetwo temperatures. and respiration rates were functions of the light intensityin the preceding light period. The function for cumulativeGDFwas of the saturation form, maximum accumulation being obtainedat 12 mW cm^–2. It is concluded that both GDF and respirationrates depend on levels of substrates formed during the lightperiod. However, the rate of GDF did not appear to be directlyrelated to the rate of respiration.