1992
DOI: 10.1007/bf00729646
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Three-dimensional visualization of confocal images of wood pulp fibres

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Cited by 8 publications
(8 citation statements)
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“…First, we evaluated the general anatomy of the stems in transverse sections at the top three axial locations (the widest stems could not be cut transverselly to preserve the plants): flexible searchers (2mm diameter), stiff thin branches (2mm diameter), and mature stems (6-10mm diameter). Stem material was maintained in 1X Tris-buffered saline (TBS), sectioned transversally at 50 μm with a Reichert-Jung Hn-40 sliding microtome (Austria), mounted onto glass slides, and stained with aniline blue that stains callose of the sieve tubes, or with 0.1% of acridine orange in TBS buffer, which yields fluorescence of the lignified tissues (Robertson et al, 1992). To sample the phloem tissue, the external side of stems containing the bark were extracted with a sharp knife at the different positions described above, kept in buffer, sectioned longitudinally with a microscalpel, and stained with aniline blue.…”
Section: Methodsmentioning
confidence: 99%
“…First, we evaluated the general anatomy of the stems in transverse sections at the top three axial locations (the widest stems could not be cut transverselly to preserve the plants): flexible searchers (2mm diameter), stiff thin branches (2mm diameter), and mature stems (6-10mm diameter). Stem material was maintained in 1X Tris-buffered saline (TBS), sectioned transversally at 50 μm with a Reichert-Jung Hn-40 sliding microtome (Austria), mounted onto glass slides, and stained with aniline blue that stains callose of the sieve tubes, or with 0.1% of acridine orange in TBS buffer, which yields fluorescence of the lignified tissues (Robertson et al, 1992). To sample the phloem tissue, the external side of stems containing the bark were extracted with a sharp knife at the different positions described above, kept in buffer, sectioned longitudinally with a microscalpel, and stained with aniline blue.…”
Section: Methodsmentioning
confidence: 99%
“…First, we evaluated the general anatomy of the stems in transverse sections at the top three axial locations (the widest stems could not be cut transversely to preserve the plants): flexible searchers (2mm diameter), stiff thin branches (2mm diameter), and mature stems (6-10mm diameter). Stem material was maintained in 1X Tris-buffered saline (TBS), sectioned transversally at 50 μm with a Reichert-Jung Hn-40 sliding microtome (Austria), mounted onto glass slides, and stained with aniline blue that binds to callose of the sieve tubes, or with 0.1% of acridine orange in TBS buffer, which yields fluorescence of the lignified tissues (Robertson et al, 1992). To sample the phloem tissue, the external side of stems containing the bark were extracted with a sharp knife at the different positions described above, kept in buffer, sectioned longitudinally with a microscalpel, and stained with aniline blue.…”
Section: Stem Anatomymentioning
confidence: 99%
“…A complete understanding of paper structure requires thus a comprehensive 3D characterization. Image acquisition for 3D reconstruction and analysis may be performed with LM (Hasuike et al , 1992; Wiltsche et al , 2005), CLSM (Robertson et al , 1992; Moss et al , 1993; Ting et al , 1997; Xu et al , 1997; Ozaki et al , 2006) and SEM (Aronsson et al , 2002; Chinga & Helle, 2003c; Chinga et al , 2004). Although SEM provides high quality and sub‐micrometre resolution, the application of SEM to 3D analysis may be time consuming and not suitable as a standard assessment method.…”
Section: Characterization Of Paper Structuresmentioning
confidence: 99%