2002
DOI: 10.1007/s00344-002-0036-x
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Primary Root Growth and the Pattern of Root Apical Meristem Organization are Coupled

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Cited by 31 publications
(22 citation statements)
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“…; Burton et al, 2013). Cortical cell files are formed by several successive asymmetric periclinal divisions in the root apical meristem (Baum et al, 2002;Chapman et al, 2003;Lux et al, 2004). It has been documented that the number of such periclinal divisions varies among species, genotypes, and root types (Lux et al, 2004;Coudert et al, 2010), which might generate differences in CCFN as observed here.…”
Section: Discussionmentioning
confidence: 52%
“…; Burton et al, 2013). Cortical cell files are formed by several successive asymmetric periclinal divisions in the root apical meristem (Baum et al, 2002;Chapman et al, 2003;Lux et al, 2004). It has been documented that the number of such periclinal divisions varies among species, genotypes, and root types (Lux et al, 2004;Coudert et al, 2010), which might generate differences in CCFN as observed here.…”
Section: Discussionmentioning
confidence: 52%
“…In the second case, of changes of meristem construction, the closed-to-open change in meristem type may be evidence of a large-scale wandering of the tensor analogue, even to the extent of its departure from the vectorial map of the root's interior; but it is more likely that the change is due to breakdown in the self-maintenance of the tensor analogue itself. The new, 'open'-type meristem then becomes destined to a final determinate phase of growth, ending with the abolition of a meristem and the cessation of root elongation (Chapman et al 2003).…”
Section: Self-maintenancementioning
confidence: 99%
“…Plant material was dehydrated in an increasing series of tertiary alcohols (50, 70, 90, 100%, three changes in the latter), embedded in Paraplast X-tra (Sigma-Aldrich, USA) [27] and cut as 5-7-μm-thick transverse sections on a rotary microtome (Leica RM2135, Leica Instruments, Germany). Sections were stained with a 1% Alcian blue-safranin O mixture (2:1) [27], or according to a modified PAS method [28]. For the latter, series of dewaxed and hydrated sections were treated with 1% periodic acid for 20 min in a water bath (40°C), thoroughly rinsed with distilled water, and stained with Schiff 's reagent (fuchsin-sulfite reagent, Sigma-Aldrich, USA) for one hour in the dark.…”
Section: Anatomical Analysesmentioning
confidence: 99%