JXB Advance Access published online on November 16, 2006
Journal of Experimental Botany, doi:10.1093/jxb/erl210
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1 Advanced Research Institute for the Sciences and Humanities, Nihon University, 6F Ichigaya Tokyu Building, 4-2-1 Kudan-kita, Chiyoda, Tokyo 102-0073, Japan
* To whom correspondence should be addressed. A passive light microscope system has been developed, capable of reconstructing an extended-focus 3-D cell-level image of chlorophyll fluorescence and
Received May 8, 2006
Accepted September 13, 2006
Imaging Stress Responses in Plants Special Issue
3-D cell-level chlorophyll fluorescence imaging of ozone-injured sunflower leaves using a new passive light microscope system
Ryosuke Endo 1 * and Kenji Omasa 2
2 Department of Biological and Environmental Engineering, Graduate School of Agricultural and Life Sciences, The University of Tokyo, 1-1-1 Yayoi, Bunkyo, Tokyo 113-8657, Japan
Ryosuke Endo, E-mail: ryosuke-endo{at}arish.nihon-u.ac.jp
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Abstract
PSII of intact attached leaves using a limited number of focal plane images of chlorophyll fluorescence. Using this system, the relationships between the depth of the mesophyll cells in spongy tissue and the intensity of the chlorophyll fluorescence and the
PSII were investigated in sunflower leaves exposed to 300 ppb ozone for 12 h at a PPFD of 300 µmol m-2 s-1 actinic light. After ozone exposure, fluorescence intensity (F) largely decreased in the cells just under the epidermal cells (within
20 µm of the epidermal cells), but the sites where fluorescence intensity decreased had no relationship to the position of the stomata. By contrast, the distribution of
PSII showed no change after the ozone exposure. These findings suggest that ozone-induced inhibition occurs in the cells just under the epidermal cells by reducing the light absorption of the chloroplasts, while the operating quantum efficiency of PSII photochemistry is maintained.![]()
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