The quantum yields of non-cyclic electron transport from photosystem II (determined from chlorophyll a fluorescence) and carbon dioxide assimilation were measured in vivo in representative species of the three subgroups of C4 plants (NADP-malic enzyme, NAD-malic enzyme and PEP-carboxykinase) over a series of intercellular CO2 concentrations (CI) at both 21% and 2% O2. The CO2 assimilation rate was independent of O2 concentration over the entire range of Ci (up to 500 μbar) in all three C4 subgroups. The quantum yield of PS II electron transport was similar, or only slightly greater, in 21% v. 2% O2 at all Ci values. In contrast, in the C3 species wheat there was a large O2 dependent increase in PS II quantum yield at low CO2, which reflects a high level of photorespiration. In the C4 plants, the relationship of the quantum yield of PS II electron transport to the quantum yield of CO2 fixation is linear suggesting that photochemical use of energy absorbed by PS II is tightly linked to CO2 fixation in C4 plants. This relationship is nearly identical in all three subgroups and may allow estimates of photosynthetic rates of C4 plants based on measurements of PS II photochemical efficiency. The results suggest that in C4 plants both the photoreduction of O2 and photorespiration are low, even at very limiting CO2 concentrations.
The partitioning of light energy absorbed by photosystem (PS) II in the C4 species maize was investigated under various photosynthetic photon flux densities (PPFD), temperatures, and intercellular CO2 concentrations. The relationship between the quantum yield of PSII electron transport (�e) and the quantum yield of CO2 assimilation (ΦCO2) was generally found to be linear, with similar slopes. This indicates that PSII electron transport is tightly coupled to CO2 assimilation such that measurements of �e may be used to estimate photosynthetic rates in maize. Coefficients of quenching of PSII chlorophyll fluorescence indicated that, under excessive PPFD or when CO2 assimilation was decreased due to suboptimal or supraoptimal temperature or low Ci, the energy in excess of that needed to drive the reduced rate of PSII electron transport was dissipated via a mechanism known to be correlated to the trans-thylakoid proton gradient (high energy quenching, qE) and a mechanism believed to arise in the PSII antenna chlorophyll (qN(slow)). At suboptimal temperature the energy dissipation was principally at the antenna level and qE was low, while at supraoptimal temperature the reverse was true. The results are discussed relative to coupling of PSII activity to CO2 fixation and mechanisms of energy dissipation in this C4 species.
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