Does the photosynthetic light-acclimation need change in leaf anatomy?

By Riichi Oguchi, K. Hikosaka, T. Hirose. 2003

377 citations recorded by the source corpus.

Subfields: Ecology, Global and Planetary Change, Plant Science

View Paper: https://www.semanticscholar.org/paper/6c0f046ad96b2e59f88cf1bb66ef3455f5fdd527

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In Ecology

In Global and Planetary Change

In Plant Science

Citations in the corpus

Blue light dose–responses of leaf photosynthesis, morphology, and chemical composition of Cucumis sativus grown under different combinations of red and blue light (2010, result): “…factor for Amax of leaves grown at an irradiance >22B. Regulation of potential Amax due to restrictions in cell size and the number of cell layers in a mature leaf as proposed by Oguchi et al. (2003) is also well in line with the correlation found between LMA and Amax in the present experiment.”
Functional leaf traits, plant communities and acclimation processes in relation to oxidative stress in trees: a critical overview (2008, background): “It is well known that, under these conditions, leaves increase their photosynthesis activity considerably, as compared with leaves growing in a steady and stable light condition (Küppers & Schneider, 1993; Naumburg & Ellsworth, 2000; Oguchi et al., 2003).”
Variation in mesophyll anatomy and photosynthetic capacity during leaf development in a deciduous mesophyte fruit tree (Prunus persica) and an evergreen sclerophyllous Mediterranean shrub (Olea europaea) (2008, background): “Oguchi et al. 2003 ), though thickness would result in less efficient CO2 transfer at full leaf area expansion.”
Environmental and developmental controls on specific leaf area are little modified by leaf allometry (2008, background): “This occurs, for instance, under high light or temperature conditions ( Oguchi, Hikosaka & Hirose 2003 ).”
Light interception and radiation use efficiency response to narrow-wide row planting patterns in maize (2012, background): “LMA is sensitive to environmental changes, especially to intercepted light ( Terashima et al., 2001; Oguchi et al., 2003).”
Physiological and structural tradeoffs underlying the leaf economics spectrum. (2017, background): “Available knowledge for the fourth component of PNUE, Sc/Np, is limited, with values ranging from 5.4 to 12.5 m2 g 1 Rubisco for three herbaceous species (Evans et al., 1994; Miyazawa & Terashima, 2001; Oguchi et al., 2003).”