The initial protrusion of a leaf primordium can form without concurrent periclinal cell divisions

1971 ◽  
Vol 49 (9) ◽  
pp. 1601-1603 ◽  
Author(s):  
Donald E. Foard

The view that periclinal cell divisions cause the initial protrusion of a leaf primordium may be tested by using ionizing radiation to prevent cell divisions without preventing growth. After receiving 800 krad of gamma rays, wheat grains containing embryos with three leaf primordia produce seedlings in which a fourth protrusion of the shoot apex forms unaccompanied by cell divisions. This protrusion without periclinal divisions occurs in the same phyllotactic position as that of the fourth leaf primordium in which periclinal divisions occur. In addition to proper phyllotactic position, the protrusion without cell divisions is formed by the outermost cell layer, as is the initial protrusion of a typical leaf primordium of wheat; moreover, the initial number of cells involved is the same in both kinds of protrusions. Therefore the fourth protrusion in seedlings from irradiated grain is interpreted as the initial protrusion of a leaf primordium that formed without periclinal cell divisions. Measured along the axis of greatest extension, the protrusions without cell divisions represent about a four- to eight-fold increase over the anticlinal dimension of the surface-cell layer in the embryo. These protrusions do not develop further. The absence of cell divisions limits the extent of primordial growth, but does not prevent its inception. Periclinal cell divisions do not cause the initial protrusion of a leaf primordium.

1967 ◽  
Vol 45 (11) ◽  
pp. 2073-2080 ◽  
Author(s):  
B. C. Sharman

At the onset of inflorescence production, the shoot apex continues to initiate leaf primordia, in the same alternating sequence of the foliage primordia below. Buds arise so precociously in the axils of the primordia that the apex appears to be producing double structures, the so-called "double ridges". The buds rapidly develop into lateral spikelets but the subtending leaf primordia remain rudimentary. After producing some 20–25 such primordia, the apex initiates the glumes and lemmas of the terminal spikelet, still continuing the same distichous sequence. Occasional deviations from the normal pattern of development seem to be the cause of some of the abnormal inflorescences which may be found: for example, the leaf primordium subtending the lowest lateral spikelet may grow out into a small foliage leaf, or the buds may grow out into side heads instead of single spikelets, or the spikelets may become abnormally elongated. Other abnormalities, such as "banana" twin spikelets and Y-forked heads are less easily "explained". The morphology of still unreported abnormalities can probably be predicted. The relative rarity of freak heads spotlights the stability of growth correlation which is achieved during the morphogenesis of normal inflorescences.


Botany ◽  
2015 ◽  
Vol 93 (9) ◽  
pp. 611-621
Author(s):  
M.D. Shafiullah ◽  
Christian R. Lacroix

Myriophyllum aquaticum (Vell.) Verdc. is heterophyllous in nature with highly dissected simple leaves consisting of several lobes. KNOX (KNOTTED1-LIKE HOMEOBOX) genes are believed to have played an important role in the evolution of leaf diversity. Up-regulation of KNOX during leaf primordium initiation can lead to leaf dissection in plants with simple leaves and, if overexpressed, can produce ectopic meristems on leaves. A previous study on KNOX gene expression in the aerial form of this species showed that this gene is expressed in the shoot apical meristem (SAM), as well as in leaf primordia P0 to P8. Based on these results, it was hypothesized that the prolonged expression of the MaKN1 (Myriophyllum aquaticum Knotted1-like homeobox) gene beyond P8, might play an important role in the generation of more lobes, longer lobes, and hydathode formation in the aquatic leaves of M. aquaticum. The technique of in situ hybridization was carried out using a previously sequenced 300 bp fragment of MaKN1 to determine the expression patterns of this gene in the shoot of aquatic forms of the plant. Expression patterns of MaKN1 revealed that the SAM and leaf primordia of aquatic forms of M. aquaticum at levels P0 (youngest) to P4 were distributed throughout these structures. The level of expression of this MaKN1 gene progressively became more localized to lobes in older leaf primordia (levels P5 to P12). Previous studies of aerial forms of this plant showed MaKN1 expression until P8. Our results with aquatic forms show that the highly dissected leaf morphology in aquatic forms was the result of the prolonged expression of MaKN1 beyond P8. This resulted in the formation of elongated and slightly more numerous lobes, and hydathodes in aquatic forms. These findings support the view that KNOX genes are important developmental regulators of leaf morphogenesis and have played an important role in the evolution of leaf forms in the plant kingdom.


Botany ◽  
2010 ◽  
Vol 88 (5) ◽  
pp. 528-536 ◽  
Author(s):  
Denis Barabé ◽  
Laura Bourque ◽  
Xiaofeng Yin ◽  
Christian Lacroix

Previous studies on palm phyllotaxis deal mainly with the mature trunk. The goals of this study are (i) to determine the relationship between the number of parastichies, the divergence angle, and the plastochrone ratio at the level of the shoot apical meristem; (ii) to examine whether there are fluctuations in the divergence angle; (iii) to interpret the significance of phyllotactic parameters with respect to the mode of growth of the apex. The tubular base of the leaf primordium is more or less asymmetrical, and completely surrounds the shoot apical meristem. The phyllotactic system corresponds to a (2, 3) conspicuous parastichy pair. The mean divergence angle per apex varies between 126.9° ± 9.3° (mean ± SD) and 135. 8° ± 8.0°. Divergence angles for all apices fluctuate within a range of 115.89° to 157.33°. The mean plastochrone ratios between apices varies from 1.35 ± 0.18 to 1.58 ± 0.12. The plastochrone ratio at each plastochrone for all apices ranges from 1.09 to 2.00. There is no correlation between the angle of divergence and the plastochrone ratio. There is a fluctuation in the value of the divergence angle that falls within the range predicted by the fundamental theorem of phyllotaxis. The high value of the ratio of the diameter of leaf primordia over the diameter of the apex, and the long plastochrone might explain the lack of correlation between certain phyllotactic parameters.


1996 ◽  
Vol 23 (5) ◽  
pp. 569 ◽  
Author(s):  
LT Evans ◽  
C Blundell

An acceleration of leaf primordium initiation by the shoot apex frequently follows floral evocation, but after varying intervals. The purpose of the experiments reported here was to define more closely the relation between this reduction of the plastochron and floral evocation, using the long day (LD) plant Lolium temulentum grown under closely controlled conditions.The acceleration begins at floral evocation, on the day after the first LD exposure, and increases after exposure to additional LDs. However, plants too young to be florally evoked by one LD nevertheless manifested an acceleration of primordium initiation, so the acceleration alone is not sufficient for evocation. Single applications of highly florigenic gibberellins (GAs), such as GA5, also accelerate the initiation of primordia and floral development, more so than does the weakly florigenic GA1. By contrast, single applications of the growth retardant Trinexapac-ethyl (CGA 163'935) to plants given one LD largely prevented the acceleration of primordium initiation but without inhibiting floral development. Thus, although the acceleration of primordium initiation by LD or by GA application is the first external sign of floral evocation in L. temulentum, it is neither a sufficient nor an essential component of it.


1993 ◽  
Vol 71 (2) ◽  
pp. 211-221 ◽  
Author(s):  
W. A. Charlton

In a number of plants, mostly woody, the components of the buds are arranged so that the laminae of the young leaves all face towards the same (upper) side of the bud, rather than towards the bud apex; in axillary buds they usually face towards the parent axis. This situation has been known for many years. For convenience, the general case is here called the rotated-lamina syndrome. There have been very few developmental investigations of how the laminae attain their unusual orientation, and these have come to different conclusions about cases in the Ulmaceae. This paper reports a detailed investigation of the syndrome in Ulmus glabra and Zelkova serrata, with comparative observations on other Ulmaceae, including cases in Celtis that do not exhibit the syndrome. The syndrome arises by different means in Ulmus and Zelkova. In Ulmus the leaf primordium is asymmetrical from the outset, the leaf blade region is obliquely dorsiventral from an early stage, and further asymmetrical growth of the leaf buttress rotates the whole leaf blade region into its final orientation as it develops. Individual shoots show heteroblastic development in progressing from bud scale to foliage leaf initiation, in increasing accentuation of the rotated-lamina syndrome, and in an increasing degree of dorsiventrality. In Zelkova, as previously described, the leaf blade region appears first as a radially symmetrical upgrowth, and it acquires dorsiventral symmetry directly in the rotated position. In Celtis spp. the lamina arises in a quite normal orientation, but reorients as it emerges from the bud. The leaf primordia of all species studied show asymmetry in other aspects, particularly in respect of stipule development, and these seem to be general features of the organisation of dorsiventral shoots. Key words: Ulmus, Zelkova, Celtis, leaf, development, dorsiventrality, lamina rotation.


Plant Methods ◽  
2017 ◽  
Vol 13 (1) ◽  
Author(s):  
Krzysztof Kucypera ◽  
Marcin Lipowczan ◽  
Anna Piekarska-Stachowiak ◽  
Jerzy Nakielski
Keyword(s):  

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