A Rapid and Simple Method for Microscopy-Based Stomata Analyses.

There are two major methodical approaches with which changes of status in stomatal pores are addressed: indirectly by measurement of leaf transpiration, and directly by measurement of stomatal apertures. Application of the former method requires special equipment, whereas microscopic images are util...

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Main Authors: Jochen F Eisele, Florian Fäßler, Patrick F Bürgel, Christina Chaban
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2016-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC5061359?pdf=render
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spelling doaj-34f8b265cabf4ade90d25b2bf736dc6d2020-11-25T00:40:23ZengPublic Library of Science (PLoS)PLoS ONE1932-62032016-01-011110e016457610.1371/journal.pone.0164576A Rapid and Simple Method for Microscopy-Based Stomata Analyses.Jochen F EiseleFlorian FäßlerPatrick F BürgelChristina ChabanThere are two major methodical approaches with which changes of status in stomatal pores are addressed: indirectly by measurement of leaf transpiration, and directly by measurement of stomatal apertures. Application of the former method requires special equipment, whereas microscopic images are utilized for the direct measurements. Due to obscure visualization of cell boundaries in intact leaves, a certain degree of invasive leaf manipulation is often required. Our aim was to develop a protocol based on the minimization of leaf manipulation and the reduction of analysis completion time, while still producing consistent results. We applied rhodamine 6G staining of Arabidopsis thaliana leaves for stomata visualization, which greatly simplifies the measurement of stomatal apertures. By using this staining protocol, we successfully conducted analyses of stomatal responses in Arabidopsis leaves to both closure and opening stimuli. We performed long-term monitoring of living stomata and were able to document the same leaf before and after treatment. Moreover, we developed a protocol for rapid-fixation of epidermal peels, which enables high throughput data analysis. The described method allows analysis of stomatal apertures with minimal leaf manipulation and usage of the same leaf for sequential measurements, and will facilitate the analysis of several lines in parallel.http://europepmc.org/articles/PMC5061359?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Jochen F Eisele
Florian Fäßler
Patrick F Bürgel
Christina Chaban
spellingShingle Jochen F Eisele
Florian Fäßler
Patrick F Bürgel
Christina Chaban
A Rapid and Simple Method for Microscopy-Based Stomata Analyses.
PLoS ONE
author_facet Jochen F Eisele
Florian Fäßler
Patrick F Bürgel
Christina Chaban
author_sort Jochen F Eisele
title A Rapid and Simple Method for Microscopy-Based Stomata Analyses.
title_short A Rapid and Simple Method for Microscopy-Based Stomata Analyses.
title_full A Rapid and Simple Method for Microscopy-Based Stomata Analyses.
title_fullStr A Rapid and Simple Method for Microscopy-Based Stomata Analyses.
title_full_unstemmed A Rapid and Simple Method for Microscopy-Based Stomata Analyses.
title_sort rapid and simple method for microscopy-based stomata analyses.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2016-01-01
description There are two major methodical approaches with which changes of status in stomatal pores are addressed: indirectly by measurement of leaf transpiration, and directly by measurement of stomatal apertures. Application of the former method requires special equipment, whereas microscopic images are utilized for the direct measurements. Due to obscure visualization of cell boundaries in intact leaves, a certain degree of invasive leaf manipulation is often required. Our aim was to develop a protocol based on the minimization of leaf manipulation and the reduction of analysis completion time, while still producing consistent results. We applied rhodamine 6G staining of Arabidopsis thaliana leaves for stomata visualization, which greatly simplifies the measurement of stomatal apertures. By using this staining protocol, we successfully conducted analyses of stomatal responses in Arabidopsis leaves to both closure and opening stimuli. We performed long-term monitoring of living stomata and were able to document the same leaf before and after treatment. Moreover, we developed a protocol for rapid-fixation of epidermal peels, which enables high throughput data analysis. The described method allows analysis of stomatal apertures with minimal leaf manipulation and usage of the same leaf for sequential measurements, and will facilitate the analysis of several lines in parallel.
url http://europepmc.org/articles/PMC5061359?pdf=render
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