Relationship between the inhibition of leaf respiration by light and enhancement of leaf dark respiration following light treatment

Abstract

Respiration (R, non-photorespiratory mitochondrial CO₂ release) in leaves is inhibited by light. However, exposure to darkness after a period of illumination can also result in R being temporarily stimulated (termed ‘light enhanced dark respiration’, LEDR). We used a fast-response CO₂ exchange system to investigate these observations in tobacco leaves. After switching off the light, there were two peaks of CO₂ release, the first at 15–20 s (the photorespiratory post-illumination burst) and the second at 180–250 s (LEDR). LEDR occurred in all post-illumination experiments, independent of O₂ or CO₂ concentration. However, LEDR increased with increasing irradiance during the pre-dark period, suggesting some dependency on prior photosynthesis. We investigated the inhibition of R by light at low CO₂ concentrations (&Ggr;_*): &Ggr;_* is the intercellular CO₂ concentration at which net CO₂ release represents R in the light. The inhibition of R in the light took about 50 s and was even evident at 3 mmol photons m^-2 s^-1, regardless of the light quality (red, blue or white). The inhibition of R by light showed similar dependency on irradiance as LEDR, such that the degree of inhibition was positively correlated with the level of LEDR. In the light, switching from 350 ppm to a low CO₂ concentration that resulted in the intercellular CO₂ concentration being at &Ggr;_*, resulted in R initially increasing and then stabilising. Maintaining the leaf at &Ggr;_* did not, therefore, lead to an underestimation of R. Our data suggest that a common mechanism may be responsible for both the inhibition of R by light and LEDR.