Irradiance and phenotype: comparative eco-development of sun and shade leaves in relation to photosynthetic CO₂ diffusion
The subject of this paper, sun leaves are thicker and show higher photosynthetic rates than the shade leaves, is approached in two ways. The first seeks to answer the question: why are sun leaves thicker than shade leaves? To do this, CO₂ diffusion within a leaf is examined first. Because affinity o...
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Published in | Journal of experimental botany Vol. 57; no. 2; pp. 343 - 354 |
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Main Authors | , , , , |
Format | Journal Article Conference Proceeding |
Language | English |
Published |
Oxford
Oxford University Press
01.01.2006
Oxford Publishing Limited (England) |
Subjects | |
Online Access | Get full text |
ISSN | 0022-0957 1460-2431 |
DOI | 10.1093/jxb/erj014 |
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Abstract | The subject of this paper, sun leaves are thicker and show higher photosynthetic rates than the shade leaves, is approached in two ways. The first seeks to answer the question: why are sun leaves thicker than shade leaves? To do this, CO₂ diffusion within a leaf is examined first. Because affinity of Rubisco for CO₂ is low, the carboxylation of ribulose 1,5-bisphosphate is competitively inhibited by O₂, and the oxygenation of ribulose 1,5-bisphosphate leads to energy-consuming photorespiration, it is essential for C₃ plants to maintain the CO₂ concentration in the chloroplast as high as possible. Since the internal conductance for CO₂ diffusion from the intercellular space to the chloroplast stroma is finite and relatively small, C₃ leaves should have sufficient mesophyll surfaces occupied by chloroplasts to secure the area for CO₂ dissolution and transport. This explains why sun leaves are thicker. The second approach is mechanistic or 'how-oriented'. Mechanisms are discussed as to how sun leaves become thicker than shade leaves, in particular, the long-distance signal transduction from mature leaves to leaf primordia inducing the periclinal division of the palisade tissue cells. To increase the mesophyll surface area, the leaf can either be thicker or have smaller cells. Issues of cell size are discussed to understand plasticity in leaf thickness. |
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AbstractList | The subject of this paper, sun leaves are thicker and show higher photosynthetic rates than the shade leaves, is approached in two ways. The first seeks to answer the question: why are sun leaves thicker than shade leaves? To do this, CO2 diffusion within a leaf is examined first. Because affinity of Rubisco for CO2 is low, the carboxylation of ribulose 1,5-bisphosphate is competitively inhibited by O2, and the oxygenation of ribulose 1,5-bisphosphate leads to energy-consuming photorespiration, it is essential for C3 plants to maintain the CO2 concentration in the chloroplast as high as possible. Since the internal conductance for CO2 diffusion from the intercellular space to the chloroplast stroma is finite and relatively small, C3 leaves should have sufficient mesophyll surfaces occupied by chloroplasts to secure the area for CO2 dissolution and transport. This explains why sun leaves are thicker. The second approach is mechanistic or 'how-oriented'. Mechanisms are discussed as to how sun leaves become thicker than shade leaves, in particular, the long-distance signal transduction from mature leaves to leaf primordia inducing the periclinal division of the palisade tissue cells. To increase the mesophyll surface area, the leaf can either be thicker or have smaller cells. Issues of cell size are discussed to understand plasticity in leaf thickness.The subject of this paper, sun leaves are thicker and show higher photosynthetic rates than the shade leaves, is approached in two ways. The first seeks to answer the question: why are sun leaves thicker than shade leaves? To do this, CO2 diffusion within a leaf is examined first. Because affinity of Rubisco for CO2 is low, the carboxylation of ribulose 1,5-bisphosphate is competitively inhibited by O2, and the oxygenation of ribulose 1,5-bisphosphate leads to energy-consuming photorespiration, it is essential for C3 plants to maintain the CO2 concentration in the chloroplast as high as possible. Since the internal conductance for CO2 diffusion from the intercellular space to the chloroplast stroma is finite and relatively small, C3 leaves should have sufficient mesophyll surfaces occupied by chloroplasts to secure the area for CO2 dissolution and transport. This explains why sun leaves are thicker. The second approach is mechanistic or 'how-oriented'. Mechanisms are discussed as to how sun leaves become thicker than shade leaves, in particular, the long-distance signal transduction from mature leaves to leaf primordia inducing the periclinal division of the palisade tissue cells. To increase the mesophyll surface area, the leaf can either be thicker or have smaller cells. Issues of cell size are discussed to understand plasticity in leaf thickness. The subject of this paper, sun leaves are thicker and show higher photosynthetic rates than the shade leaves, is approached in two ways. The first seeks to answer the question: why are sun leaves thicker than shade leaves? To do this, CO₂ diffusion within a leaf is examined first. Because affinity of Rubisco for CO₂ is low, the carboxylation of ribulose 1,5-bisphosphate is competitively inhibited by O₂, and the oxygenation of ribulose 1,5-bisphosphate leads to energy-consuming photorespiration, it is essential for C₃ plants to maintain the CO₂ concentration in the chloroplast as high as possible. Since the internal conductance for CO₂ diffusion from the intercellular space to the chloroplast stroma is finite and relatively small, C₃ leaves should have sufficient mesophyll surfaces occupied by chloroplasts to secure the area for CO₂ dissolution and transport. This explains why sun leaves are thicker. The second approach is mechanistic or 'how-oriented'. Mechanisms are discussed as to how sun leaves become thicker than shade leaves, in particular, the long-distance signal transduction from mature leaves to leaf primordia inducing the periclinal division of the palisade tissue cells. To increase the mesophyll surface area, the leaf can either be thicker or have smaller cells. Issues of cell size are discussed to understand plasticity in leaf thickness. The subject of this paper, sun leaves are thicker and show higher photosynthetic rates than the shade leaves, is approached in two ways. The first seeks to answer the question: why are sun leaves thicker than shade leaves? To do this, CO2 diffusion within a leaf is examined first. Because affinity of Rubisco for CO2 is low, the carboxylation of ribulose 1,5-bisphosphate is competitively inhibited by O2, and the oxygenation of ribulose 1,5-bisphosphate leads to energy-consuming photorespiration, it is essential for C3 plants to maintain the CO2 concentration in the chloroplast as high as possible. Since the internal conductance for CO2 diffusion from the intercellular space to the chloroplast stroma is finite and relatively small, C3 leaves should have sufficient mesophyll surfaces occupied by chloroplasts to secure the area for CO2 dissolution and transport. This explains why sun leaves are thicker. The second approach is mechanistic or 'how-oriented'. Mechanisms are discussed as to how sun leaves become thicker than shade leaves, in particular, the long-distance signal transduction from mature leaves to leaf primordia inducing the periclinal division of the palisade tissue cells. To increase the mesophyll surface area, the leaf can either be thicker or have smaller cells. Issues of cell size are discussed to understand plasticity in leaf thickness. |
Author | Yano, Satoshi Hanba, Yuko T Terashima, Ichiro Tazoe, Youshi Vyas, Poonam |
Author_xml | – sequence: 1 fullname: Terashima, Ichiro – sequence: 2 fullname: Hanba, Yuko T – sequence: 3 fullname: Tazoe, Youshi – sequence: 4 fullname: Vyas, Poonam – sequence: 5 fullname: Yano, Satoshi |
BackLink | http://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17508525$$DView record in Pascal Francis https://www.ncbi.nlm.nih.gov/pubmed/16356943$$D View this record in MEDLINE/PubMed |
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Keywords | resistance to CO2 diffusion diffusion Intercellular space Enzyme Carbon dioxide Ribulose-bisphosphate carboxylase intercellular spaces Stomata chloroplasts Lyases Plant leaf Leaf area conductance Cell wall Signal transduction mechanical strength Carbon-carbon lyases Photorespiration Carboxy-lyases Development Photosynthesis Aquaporin Chloroplast |
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Snippet | The subject of this paper, sun leaves are thicker and show higher photosynthetic rates than the shade leaves, is approached in two ways. The first seeks to... |
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SubjectTerms | acclimation Agricultural and forest climatology and meteorology. Irrigation. Drainage Agricultural and forest meteorology Agronomy. Soil science and plant productions Amaranthus - anatomy & histology Amaranthus - growth & development Amaranthus - metabolism Aquaporin Aquaporins - physiology Biological and medical sciences C3 plants Carbon - metabolism Carbon dioxide Carbon Dioxide - metabolism cell division Cell Membrane - physiology cell wall Cell Wall - physiology chloroplasts Chloroplasts - metabolism Chloroplasts - ultrastructure Climatic adaptation. Acclimatization conductance Diffusion Ecosystem Fagus - anatomy & histology Fagus - growth & development Fagus - metabolism Fundamental and applied biological sciences. Psychology gas exchange General agronomy. Plant production intercellular spaces leaf primordia Leaves Light light intensity literature reviews mechanical strength mesophyll Oxygen - metabolism Oxygenation Phenotype photorespiration Photosynthesis plant development Plant Leaves - anatomy & histology Plant Leaves - growth & development Plant Leaves - metabolism Plant Physiological Phenomena plants resistance to CO2 diffusion ribulose 1,5-diphosphate ribulose-bisphosphate carboxylase Ribulose-Bisphosphate Carboxylase - metabolism Ribulosephosphates - metabolism shade signal transduction stomata surface area thickness |
Title | Irradiance and phenotype: comparative eco-development of sun and shade leaves in relation to photosynthetic CO₂ diffusion |
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