2009
DOI: 10.1016/j.jbiosc.2008.10.001
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Classification of pollen species using autofluorescence image analysis

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Cited by 56 publications
(43 citation statements)
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“…It is evident from row (A) that there is no autofl uorescence of natural spores with these settings, whereas the blue and red channels show strong autofl uorescence from the spore constituents which is even more evident from their overlay image. This autofl uorescence can be primarily attributed to the presence of sporoplasm constituents in the form of cellular organelles, [ 16,38,39 ] and suggests that a large portion of the inner cavity of the natural spores is empty.…”
Section: Macromolecular Encapsulation and Characterization Of Naturalmentioning
confidence: 99%
“…It is evident from row (A) that there is no autofl uorescence of natural spores with these settings, whereas the blue and red channels show strong autofl uorescence from the spore constituents which is even more evident from their overlay image. This autofl uorescence can be primarily attributed to the presence of sporoplasm constituents in the form of cellular organelles, [ 16,38,39 ] and suggests that a large portion of the inner cavity of the natural spores is empty.…”
Section: Macromolecular Encapsulation and Characterization Of Naturalmentioning
confidence: 99%
“…Such chemotaxonomy is possible because the tissues of plants that utilize the C 4 photosynthetic pathway, which has independently evolved at least 18 times in grasses (Edwards et al 2010), have a heavier carbon isotopic composition than the tissues of plants that use the C 3 photosynthetic pathway (Amundson et al 1997;Vogts et al 2009). Techniques based on the fluorescence properties of the exine have also been explored, and the fluorescence spectra emitted from the exine following excitation can differ between certain taxa, which has been used to classify pollen grains (Mitsumoto et al 2009;Pan et al 2011).…”
Section: The Use Of Nonmorphological Charactersmentioning
confidence: 99%
“…17,18 Fluorescence and bright-field micrographs of pollen grains on a glass plate were taken using a fluorescence microscope (Leica DMR; Leica Microsystems, Tokyo, Japan) equipped with both an ultraviolet illuminating system using a xenon lamp and a band-pass filter (central wavelength: 340 nm) and CCD camera (SPOT ISA-CE Color; Diagnostic Instruments, Inc, Sterling Heights, MI). Samples for scanning electron microscopy study were prepared according to the method of Vinckier and Smets.…”
Section: Microscopic Observationsmentioning
confidence: 99%