Topic
Photosynthetic capacity
About: Photosynthetic capacity is a research topic. Over the lifetime, 3898 publications have been published within this topic receiving 192610 citations.
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TL;DR: Various aspects of the biochemistry of photosynthetic carbon assimilation in C3 plants are integrated into a form compatible with studies of gas exchange in leaves.
Abstract: Various aspects of the biochemistry of photosynthetic carbon assimilation in C3 plants are integrated into a form compatible with studies of gas exchange in leaves. These aspects include the kinetic properties of ribulose bisphosphate carboxylase-oxygenase; the requirements of the photosynthetic carbon reduction and photorespiratory carbon oxidation cycles for reduced pyridine nucleotides; the dependence of electron transport on photon flux and the presence of a temperature dependent upper limit to electron transport. The measurements of gas exchange with which the model outputs may be compared include those of the temperature and partial pressure of CO2(p(CO2)) dependencies of quantum yield, the variation of compensation point with temperature and partial pressure of O2(p(O2)), the dependence of net CO2 assimilation rate on p(CO2) and irradiance, and the influence of p(CO2) and irradiance on the temperature dependence of assimilation rate.
7,312 citations
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TL;DR: Surviving in certain environments clearly does not require maximising photosynthetic capacity for a given leaf nitrogen content, as variation reflects different strategies of nitrogen partitioning, the electron transport capacity per unit of chlorophyll and the specific activity of RuBP carboxylase.
Abstract: The photosynthetic capacity of leaves is related to the nitrogen content primarily bacause the proteins of the Calvin cycle and thylakoids represent the majority of leaf nitrogen. To a first approximation, thylakoid nitrogen is proportional to the chlorophyll content (50 mol thylakoid N mol-1 Chl). Within species there are strong linear relationships between nitrogen and both RuBP carboxylase and chlorophyll. With increasing nitrogen per unit leaf area, the proportion of total leaf nitrogen in the thylakoids remains the same while the proportion in soluble protein increases. In many species, growth under lower irradiance greatly increases the partitioning of nitrogen into chlorophyll and the thylakoids, while the electron transport capacity per unit of chlorophyll declines. If growth irradiance influences the relationship between photosynthetic capacity and nitrogen content, predicting nitrogen distribution between leaves in a canopy becomes more complicated. When both photosynthetic capacity and leaf nitrogen content are expressed on the basis of leaf area, considerable variation in the photosynthetic capacity for a given leaf nitrogen content is found between species. The variation reflects different strategies of nitrogen partitioning, the electron transport capacity per unit of chlorophyll and the specific activity of RuBP carboxylase. Survival in certain environments clearly does not require maximising photosynthetic capacity for a given leaf nitrogen content. Species that flourish in the shade partition relatively more nitrogen into the thylakoids, although this is associated with lower photosynthetic capacity per unit of nitrogen.
2,973 citations
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TL;DR: In this paper, a two-stream approximation model of radiative transfer was used to calculate values of hemispheric canopy reflectance in the visible and near-infrared wavelength intervals.
Abstract: A two-stream approximation model of radiative transfer is used to calculate values of hemispheric canopy reflectance in the visible and near-infrared wavelength intervals. Simple leaf models of photosynthesis and stomatal resistance are integrated over leaf orientation and canopy depth to obtain estimates of canopy photosynthesis and bulk stomatal or canopy resistance. The ratio of near-infrared and visible reflectances is predicted to be a near linear indicator of minimum canopy resistance and photosynthetic capacity but a poor predictor of leaf area index or biomass.
2,198 citations
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TL;DR: Adaptation to irradiance level is explored, focusing on traits whose significance would be elusive if considered in terms of their impact at the leaf level alone, and three energetic tradeoffs likely to shape such adaptation are outlined, involving the economics of gas exchange, support, and biotic interactions.
Abstract: Whole-plant energy capture depends not only on the photosynthetic response of individual leaves, but also on their integration into an effective canopy, and on the costs of producing and maintaining their photosynthetic capacity. This paper explores adaptation to irradiance level in this context, focusing on traits whose significance would be elusive if considered in terms of their impact at the leaf level alone. I review traditional approaches used to demonstrate or suggest adaptation to irradiance level, and outline three energetic tradeoffs likely to shape such adaptation, involving the economics of gas exchange, support, and biotic interactions. Recent models using these tradeoffs to account for trends in leaf nitrogen content, stornatal conductance, phyllotaxis, and defensive allocations in sun v. shade are evaluated. A re-evaluation of the classic study of acclimation of the photosynthetic light response in Atriplex, crucial to interpreting adaptation to irradiance in many traits, shows that it does not completely support the central dogma of adaptation to sun v. shade unless the results are analysed in terms of whole-plant energy capture. Calculations for Liriodendron show that the traditional light compensation point has little meaning for net carbon gain, and that the effective compensation point is profoundly influenced by the costs of night leaf respiration, leaf construction, and the construction of associated support and root tissue. The costs of support tissue are especially important, raising the effective compensation point by 140 pmol m- s - ' in trees 1 m tall, and by nearly 1350 pmol m - s - ' in trees 30 m tall. Effective compensation points give maximum tree heights as a function of irradiance, and shade tolerance as a function of tree height; calculations of maximum permissible height in Liriodendron correspond roughly with the height of the tallest known individual. Finally, new models for the evolution of canopy width/height ratio in response to irradiance and coverage within a tree stratum, and for the evolution of mottled leaves as a defensive measure in understory herbs, are outlined.
1,712 citations
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TL;DR: Although trends agree with parallel summaries of enclosure studies, important quantitative differences emerge that have important implications both for predicting the future terrestrial biosphere and understanding how crops may need to be adapted to the changed and changing atmosphere.
Abstract: Atmospheric CO(2) concentration ([CO(2)]) is now higher than it was at any time in the past 26 million years and is expected to nearly double during this century. Terrestrial plants with the C(3) photosynthetic pathway respond in the short term to increased [CO(2)] via increased net photosynthesis and decreased transpiration. In the longer term this increase is often offset by downregulation of photosynthetic capacity. But much of what is currently known about plant responses to elevated [CO(2)] comes from enclosure studies, where the responses of plants may be modified by size constraints and the limited life-cycle stages that are examined. Free-Air CO(2) Enrichment (FACE) was developed as a means to grow plants in the field at controlled elevation of CO(2) under fully open-air field conditions. The findings of FACE experiments are quantitatively summarized via meta-analytic statistics and compared to findings from chamber studies. Although trends agree with parallel summaries of enclosure studies, important quantitative differences emerge that have important implications both for predicting the future terrestrial biosphere and understanding how crops may need to be adapted to the changed and changing atmosphere.
1,566 citations