Etude de la teneur en DNA nucléaire dans le méristème apical des tiges du Celosia cristata (Amarantacées) en fonction de la photopériode

1979 ◽  
Vol 57 (24) ◽  
pp. 2760-2765 ◽  
Author(s):  
D. Driss-Ecole

Two samples of plants of Celosia cristata, a quantitative short-day plant, were grown in an 8-h or a 16-h day. The shoot apices were collected at 11, 15, 18, and 28 days in order to carry out a cytophotometric study of the nuclear DNA in the corpus. This distribution of the DNA values was analyzed statistically using the χ2 test. At the beginning of development, for both 8-h day and 16-h day plants, the DNA content of the majority of the nuclei is at the 2C level. Then the percentage 2C–4C or 4C nuclei increases, slowly for the plants grown under a 16-h photoperiod and quickly for the others. At the 28th day, the Gaussian distribution of DNA values indicates that the state reached by the meristems is quite different. Between the 18th day and the 28th day of culture, ontogenesis of the shoot apex goes through a critical period. At the end of this period, shoot apices of the plants grown under a 16-h photoperiod are in the intermediate phase with a majority of nuclei in the synthetic phase (S) or in the postsynthetic phase (G2). Simultaneously, structural modifications of the axial zone give rise to a central zone characteristic of the fasciation of the shoot apex. In plants grown with an 8-h photoperiod, the shoot apex goes through the prefloral phase with more numerous nuclei in the presynthetic phase (G1) or in the synthetic one (S). For each sample the nuclei clustered in a particular phase of the cell cycle indicate that a certain synchronism of the cell cycles in the corpus takes place. These results are compared with those recently obtained by other authors working with different plants.

1969 ◽  
Vol 47 (9) ◽  
pp. 1367-1375 ◽  
Author(s):  
T. A. Steeves ◽  
M. Anne Hicks ◽  
J. M. Naylor ◽  
Patricia Rennie

The vegetative shoot apex of Helianthus annuus contains a central zone in which the cell nuclei are relatively large and stain faintly in the Feulgen reaction. Excised apices in the vegetative state were supplied with thymidine-H3 through their sterile, liquid culture medium. Autoradiography after 24 or 48 hours of feeding revealed no significant incorporation of the labeled precursor into central zone nuclei, but extensive incorporation in peripheral regions of the apex. It is concluded that during vegetative growth deoxyribonucleic acid (DNA) synthesis and mitosis are arrested in the central zone or reduced to an extremely slow rate. Microspectrophotometry, however, indicates that the central zone nuclei are not held at the 2C level. With the onset of flowering, cytological zonation disappears in the apex and the incorporation of thymidine-H3 is uniformly heavy throughout the apical region.


2016 ◽  
Vol 85 (4) ◽  
Author(s):  
Takuya Okabe

Phyllotaxis studies published in German in the 1930s have reported intriguing regularity in the arrangement of incipient leaves on shoot apices of a wide variety of plant species. However, these studies have received little attention today, even though they provide a crucial evidence base for understanding this mathematical phenomena. Here I recapitulate the essential point by means of illustrative examples. It is emphasized that accurate control of apical divergence angle is at the heart of the numerical riddle of spiral phyllotaxis. The accurate patterning at the shoot apex has an unexpected evolutionary benefit of being optimally adaptive in the subsequent events of phyllotactic change to occur on an elongating shoot.


1972 ◽  
Vol 14 (4) ◽  
pp. 773-783 ◽  
Author(s):  
T. Mohandas ◽  
W. F. Grant

The cytological effects of 2,4-D and amitrole were studied for 12 species (Tradescantia clone 02, Allium cepa, Vicia faba, Triticum aestivum, T. dicoccum, Hordeum vulgare, Secale cereale, Centaurea jacea, Cirsium vulgare, Chrysanthemum leucanthemum, Plantago major and Erigeron canadensis). Ethyl methane sulfonate (EMS) was used as a positive control. The cytological abnormalities induced in root-tip cells by both 2,4-D and amitrole included chromosome bridges, fragments, lagging chromosomes, and chromatin bodies; 2,4-D also induced chromosome contraction, and C-mitoses. Studies following seed treatments of Hordeum vulgare on M2 seedlings showed that 2,4-D and EMS induced albina mutants. Interphase nuclear volumes of the various species were measured from root-tip meristems. Nuclear DNA values were determined cytophotometrically for seven species. The relative DNA values were found to be positively correlated with nuclear volumes. The lack of any clear relationship between the number of cytological abnormalities induced by the chemicals and the nuclear and interphase chromosome volumes of the plants probably reflects a lack of synchrony of the treated cell population.


1979 ◽  
Vol 57 (8) ◽  
pp. 971-980 ◽  
Author(s):  
E. L. Davis ◽  
Patricia Rennie ◽  
Taylor A. Steeves

The cytologically distinctive central zone of the vegetative shoot apex of Helianthus annuus L. cv. Peredovic has a mitotic frequency considerably lower than that of the surrounding peripheral zone in intact plants. Apices excised and grown in culture for 5 days before being supplied with [H3]thymidine reveal a correspondingly low level of DNA synthesis in the central zone when autoradiographed. In similarly cultured apices, mitotic activity in the central zone is less than that recorded for intact plants. Labelling immediately after excision of the apex indicates that the central zone cells are activated by the operation and quiescence returns during the following 5 days. This activation is confirmed by mitotic counts 2 days after excision. The removal of only two young leaves from the apical buds of otherwise intact plants results in a comparable stimulation of mitotic activity in the central zone. These observations cast doubt upon the significance of mitotic activity in living shoot apices when these have been exposed for observation by removal of leaves. They also raise questions about the validity of labelling techniques which involve the partial dissection of the shoot apex.


2018 ◽  
Vol 83 (02) ◽  
pp. 191-197 ◽  
Author(s):  
Xueyin Yuan ◽  
Chao Gao ◽  
Jing Gao

AbstractThe phase transitions involving calcite (CaCO3-I), CaCO3-II, CaCO3-III and CaCO3-IIIb were investigated using a diamond anvil cell and micro-Raman spectroscopy. Based on the results obtained from in situ observations and Raman measurements made with six natural calcite crystals, the phase transition from calcite to CaCO3-II took place between 1.56 and 1.67 GPa under ambient temperature. Under a precise pressure of 1.97 ± 0.03 GPa, three CaCO3 samples were observed to transform from CaCO3-II directly to CaCO3-III, while in the other three samples both CaCO3-III and CaCO3-IIIb crystal structures were detected. Transformation from CaCO3-IIIb to CaCO3-III was completed in a short period in one sample, whereas in the other two samples coexistence of CaCO3-III and CaCO3-IIIb was observed over a wide pressure range from 1.97 to 3.38 GPa, with sluggish transformation from CaCO3-IIIb to CaCO3-III being observed after the samples were preserved under 3.38 GPa for 72 h. Hence, it can be concluded that CaCO3-IIIb is a metastable intermediate phase occurring during the reconstructive transformation from CaCO3-II to CaCO3-III. Splitting of the C–O in-plane bending (ν4) and symmetric stretching (ν1) vibrations and appearance of new lattice vibrations in the Raman spectra of CaCO3-III and CaCO3-IIIb suggest a lowering in crystal symmetry during the transformation from CaCO3-II through CaCO3-IIIb to CaCO3-III, which is in good agreement with the observed sequence of phase symmetries.


1981 ◽  
Vol 59 (8) ◽  
pp. 1367-1372 ◽  
Author(s):  
D. Driss-Ecole

In vitro development of fasciation was achieved from the excised shoot apices of Celosia cristata in a 16-h photoperiod. An 8-h photoperiod produced no development. The explants consisted of the meristematic dome with two leaf primordia. The best results were obtained with a nutrient medium composed of Murashige and Skoog salt mixture, 30 g/L sucrose, 5 g/L agar, and 1 mg/L indoleacetic acid (IAA). Isolated shoot apices developed callus at the bases of the explants and numerous leaves on one, two, or three flattened and fasciated meristems. Root initiation occurred sometimes but only after a long period of culture.


Pathology ◽  
1995 ◽  
Vol 27 (1) ◽  
pp. 5-7
Author(s):  
Yosuke Adachi ◽  
Masaki Mori ◽  
Masaru Haraguchi ◽  
Keizo Sugimachi ◽  
Masazumi Tsuneyoshi

1967 ◽  
Vol 45 (7) ◽  
pp. 955-959 ◽  
Author(s):  
Sidki Sadik ◽  
J. L. Ozbun

Cauliflower plants were induced to flower after being grown at 42 °F for varying periods of time, depending on the cultivar. Some of the histochemical changes in the shoot apex at the beginning of, during, and after floral induction were studied. During floral induction there is about a 20-fold increase in the volume of nucleoli and about a 3-fold increase in volume of nuclei. Apices of vegetative plants stained with bromophenol blue at pH 2.3, show small and dense nucleoli, dense and granular nuclei, and a small amount of weakly staining cytoplasm. In contrast, cells of apices of induced plants stained with bromophenol blue at pH 2.3, show large and dense nucleoli, large and weakly staining nuclei; however, these cells contain more and denser cytoplasm. Sections of vegetative and induced apices stained with alkaline fast green stained differently from those stained with bromophenol blue. Nucleoli did not stain and cytoplasm stained faintly with fast green while chromosomes stained strongly. Deoxyribonucleic acid (DNA) content of vegetative and induced apices are similar. Shoot apices of vegetative plants contained little or no starch. However, shoot apices of plants grown at 42 °F accumulate large amounts of starch. Floral primordia which develop into functional flowers are glutted with starch, while floral primordia which abort are void of starch.


1998 ◽  
Vol 76 (1) ◽  
pp. 157-165 ◽  
Author(s):  
Jérôme Thibault

Flow cytometry (FCM) has been used to estimate the nuclear DNA content of 11 Salix species and 5 hybrids. One hundred and sixty nine individuals were studied including 159 individuals from a sequence of 32 communities along a stretch of river in France and 10 individuals from French and English collections for comparison. Isolated nuclei were stained with propidium iodide. FCM was a significantly more practical and rapid technique than that of establishing the karyotype to survey many samples of Salix for variation in ploidy. The 2C DNA amounts for diploid species ranged from 0.76 to 0.98 pg, and tetraploid values ranged from 1.62 to 1.80 pg. The DNA values were consistent with the known ploidy levels. With the exception of a doubtful Salix xquercifolia, ploidy levels and DNA amounts of hybrids were intermediate compared with those of their parents. Intraspecific variation of nuclear DNA values including instrumental variation was low (i.e., 6-11% at the same ploidy level). FCM appeared to be an accurate tool for determination of Salix triploid hybrids. However, it remains limited concerning hybrids from crosses between species of the same ploidy level. Results suggest that natural hybridization might not be frequent in the communities studied, although they have been subject to disturbance. Previous overestimates of hybridization frequency in willows were probably due to misinterpretation of the effects of the environment on Salix spp. morphology; however, the extent and mechanisms of introgression in the genus remain to be further investigated. Key words: flow cytometry, Salix, hybridization, nuclear DNA content, riparian vegetation, disturbance.


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