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Summary: Theoretically, the PEP‐CK C4 subtype has a higher quantum yield of CO2 assimilation (ΦCO2) than NADP‐ME or NAD‐ME subtypes because ATP required for operating the CO2‐concentrating mechanism is believed to mostly come from the mitochondrial electron transport chain (mETC). However, reported ΦCO2 is not higher in PEP‐CK than in the other subtypes. We hypothesise, more photorespiration, associated with higher leakiness and O2 evolution in bundle‐sheath (BS) cells, cancels out energetic advantages in PEP‐CK species.Nine species (two to four species per subtype) were evaluated by gas exchange, chlorophyll fluorescence, and two‐photon microscopy to estimate the BS conductance (gbs) and leakiness using a biochemical model.Average gbs estimates were 2.9, 4.8, and 5.0 mmol m−2 s−1 bar−1, and leakiness values were 0.129, 0.179, and 0.180, in NADP‐ME, NAD‐ME, and PEP‐CK species, respectively. The BS CO2 level was somewhat higher, O2 level was marginally lower, and thus, photorespiratory loss was slightly lower, in NADP‐ME than in NAD‐ME and PEP‐CK species. Differences in these parameters existed among species within a subtype, and gbs was co‐determined by biochemical decarboxylating sites and anatomical characteristics.Our hypothesis and results partially explain variations in observed ΦCO2, but suggest that PEP‐CK species probably use less ATP from mETC than classically defined PEP‐CK mechanisms. [ABSTRACT FROM AUTHOR]

Summary Certain species in the Brassicaceae family exhibit high photosynthesis rates, potentially providing a valuable route toward improving agricultural productivity. However, factors contributing to their high photosynthesis rates are still unknown. We compared Hirschfeldia incana, Brassica nigra, Brassica rapa and Arabidopsis thaliana, grown under two contrasting light intensities. Hirschfeldia incana matched B. nigra and B. rapa in achieving very high photosynthesis rates under high growth‐light condition, outperforming A. thaliana. Photosynthesis was relatively more limited by maximum photosynthesis capacity in H. incana and B. rapa and by mesophyll conductance in A. thaliana and B. nigra. Leaf traits such as greater exposed mesophyll specific surface enabled by thicker leaf or high‐density small palisade cells contributed to the variation in mesophyll conductance among the species. The species exhibited contrasting leaf construction strategies and acclimation responses to low light intensity. High‐light plants distributed Chl deeper in leaf tissue, ensuring even distribution of photosynthesis capacity, unlike low‐light plants. Leaf anatomy of H. incana, B. nigra and B. rapa facilitated effective CO2 diffusion, efficient light use and provided ample volume for their high maximum photosynthetic capacity, indicating that a combination of adaptations is required to increase CO2‐assimilation rates in plants. [ABSTRACT FROM AUTHOR]

Grain filling is a critical process for improving crop production under adverse conditions caused by climate change. Here, using a quantitative method, we quantified post-anthesis source-sink relationships of a large data set to assess the contribution of remobilized pre-anthesis assimilates to grain growth for both biomass and nitrogen. The data set came from 13 years' semi-controlled field experimentation, in which six bread wheat genotypes were grown at plot scale under contrasting temperature, water, and nitrogen regimes. On average, grain biomass was ~10% higher than post-anthesis aboveground biomass accumulation across regimes and genotypes. Overall, the estimated relative contribution (%) of remobilized assimilates to grain biomass became increasingly significant with increasing stress intensity, ranging from virtually nil to 100%. This percentage was altered more by water and nitrogen regimes than by temperature, indicating the greater impact of water or nitrogen regimes relative to high temperatures under our experimental conditions. Relationships between grain nitrogen demand and post-anthesis nitrogen uptake were generally insensitive to environmental conditions, as there was always significant remobilization of nitrogen from vegetative organs, which helped to stabilize the amount of grain nitrogen. Moreover, variations in the relative contribution of remobilized assimilates with environmental variables were genotype-dependent. Our analysis provides an overall picture of post-anthesis source-sink relationships and pre-anthesis assimilate contributions to grain filling across (non-)environmental factors, and highlights that designing wheat adaption to climate change should account for complex multi-factor interactions., (© The Author(s) 2024. Published by Oxford University Press on behalf of the Society for Experimental Biology.)

Theoretically, the PEP-CK C 4 subtype has a higher quantum yield of CO 2 assimilation ( Φ CO 2 ) than NADP-ME or NAD-ME subtypes because ATP required for operating the CO 2 -concentrating mechanism is believed to mostly come from the mitochondrial electron transport chain (mETC). However, reported Φ CO 2 is not higher in PEP-CK than in the other subtypes. We hypothesise, more photorespiration, associated with higher leakiness and O 2 evolution in bundle-sheath (BS) cells, cancels out energetic advantages in PEP-CK species. Nine species (two to four species per subtype) were evaluated by gas exchange, chlorophyll fluorescence, and two-photon microscopy to estimate the BS conductance (g bs ) and leakiness using a biochemical model. Average g bs estimates were 2.9, 4.8, and 5.0 mmol m -2  s -1  bar -1 , and leakiness values were 0.129, 0.179, and 0.180, in NADP-ME, NAD-ME, and PEP-CK species, respectively. The BS CO 2 level was somewhat higher, O 2 level was marginally lower, and thus, photorespiratory loss was slightly lower, in NADP-ME than in NAD-ME and PEP-CK species. Differences in these parameters existed among species within a subtype, and g bs was co-determined by biochemical decarboxylating sites and anatomical characteristics. Our hypothesis and results partially explain variations in observed Φ CO 2 , but suggest that PEP-CK species probably use less ATP from mETC than classically defined PEP-CK mechanisms., (© 2024 The Authors New Phytologist © 2024 New Phytologist Foundation.)

Leaf day respiration (R d ) strongly influences carbon-use efficiencies of whole plants and the global terrestrial biosphere. It has long been thought that R d is slower than respiration in the dark at a given temperature, but measuring R d by gas exchange remains a challenge because leaves in the light are also photosynthesizing. The Kok method and the Laisk method are widely used to estimate R d . We highlight theoretical limitations of these popular methods, and recent progress toward their improvement by using additional information from chlorophyll fluorescence and by accounting for the photosynthetic reassimilation of respired CO 2 . The latest evidence for daytime CO 2 and energy release from the oxidative pentose phosphate pathway in chloroplasts appears to be important to understanding R d ., (© 2023 The Authors New Phytologist © 2023 New Phytologist Foundation.)