Abstract
A fundamental challenge in plant physiology is independently determining the rates of gross O(2) production by photosynthesis and O(2) consumption by respiration, photorespiration, and other processes. Previous studies on isolated chloroplasts or leaves have separately constrained net and gross O(2) production (NOP and GOP, respectively) by labeling ambient O(2) with (18)O while leaf water was unlabeled. Here, we describe a method to accurately measure GOP and NOP of whole detached leaves in a cuvette as a routine gas-exchange measurement. The petiole is immersed in water enriched to a δ(18)O of ∼9,000‰, and leaf water is labeled through the transpiration stream. Photosynthesis transfers (18)O from H(2)O to O(2) GOP is calculated from the increase in δ(18)O of O(2) as air passes through the cuvette. NOP is determined from the increase in O(2)/N(2) Both terms are measured by isotope ratio mass spectrometry. CO(2) assimilation and other standard gas-exchange parameters also were measured. Reproducible measurements are made on a single leaf for more than 15 h. We used this method to measure the light response curve of NOP and GOP in French bean (Phaseolus vulgaris) at 21% and 2% O(2) We then used these data to examine the O(2)/CO(2) ratio of net photosynthesis, the light response curve of mesophyll conductance, and the apparent inhibition of respiration in the light (Kok effect) at both oxygen levels. The results are discussed in the context of evaluating the technique as a tool to study and understand leaf physiological traits.